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Showing 20 of 27881 trials
Identification and Evaluation of Patients at Risk of Developing Cardiotoxicity After Receiving Chemotherapy for Breast Cancer, Lymphoma or Leukemia
NCT04541212
Active, positions filled
Conditions Breast Cancer, Lymphoma, Leukemia
Phase Not Applicable
Enrollment 169
Locations 6 sites
Compensation Compensation varies
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

This is an observational study of the occurrence of cardiac toxicity in patients with breast cancer,lymphoma or leukemia receiving chemotherapy including an anthracycline. Patients will be identified at the oncology clinic and will be included in the study if all eligible criteria are met. The study will involve retrospective and prospective evaluations. Safety will be assessed through reporting of serious adverse events (SAEs) related to study procedures.

Design

Study type: Observational Observational model: Cohort Time perspective: Other

Interventions / Regimen

  • Diagnostic Test: Cardiac Imaging — Cardiac Imaging: echography, ECG, MRI Blood tests: Lipid profile, hs-CRP, metabolic markers, HDL functionality, pharmacogenetic testing (optional), hematocrit, pregnancy test
  • Other: Data Collection — Collection of retrospective data

Primary Outcomes

  • Myocardial extracellular volume (ECV) (Change from baseline to 3, 6, 12,and 24 months)
  • Myocardial extracellular volume (ECV) (Change from baseline to prior study entry, 12 and 24 months post study entry.)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: OBSERVATIONAL
Phase: Not Applicable
Status: Active, positions filled
Start Date: 2021-12-02
Completion: 2027-09-30
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: Not specified
Enrollment: 169 (ACTUAL)
Sponsor & Investigators
Lead Sponsor: Montreal Heart Institute
Collaborators: AstraZeneca
Principal Investigators:
  • Jean-Claude Tardif, MD (PRINCIPAL_INVESTIGATOR) - Montreal Heart Institute
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Diagnostic Test: Cardiac Imaging — Cardiac Imaging: echography, ECG, MRI Blood tests: Lipid profile, hs-CRP, metabolic markers, HDL functionality, pharmacogenetic testing (optional), hematocrit, pregnancy test
  • Other: Data Collection — Collection of retrospective data
Study Locations (6 sites)
Centre Hospitalier de l'université de Montréal (CHUM), Montreal, Quebec H2X0C1 Canada
CIUSSS Ouest de l'ile de Montreal - St-Mary's Hospital, Montreal, Quebec H3T 1M5 Canada
CIUSSS de l'Est-de-l'Île-de-Montréal - Hôpital Maisonneuve-Rosemont, Montreal, Quebec Canada
CIUSSS du Centre-Ouest de l'Île de Montréal - Jewish General Hospital, Montreal, Quebec Canada
Montreal Heart Institute, Montreal, Quebec Canada
CISSSS de Lanaudière_Hôpital Pierre LeGardeur (referring site), Terrebonne, Quebec (QC) J6V 2H2 Canada
Eligibility Criteria
Inclusion Criteria: * Age 18 years or older at time of CT initiation * Signed informed consent * Patients with diagnosis of breast cancer,lymphoma or leukemia (including autografted subjects) * Planned, ongoing or completed (within last 5 years) chemotherapy with anthracycline * Left ventricular ejection fraction (LVEF) ≥50% pre-chemotherapy * The participant is willing to undergo CMR scans and all other required study procedures Exclusion Criteria: * Known cardiomyopathy and/or LVEF \<50% * Known heart failure * History of myocardial infarction (MI) * Clinically significant cardiac valvular disease * Clinically significant pericardial effusion * Allografted subjects * Contraindications to CMR testing (Cohort A \& prospective evaluation for Cohort B): * Pacemakers, other metallic implants or severe claustrophobia * Weight \> 135 kg * Patients with a history of previous allergic reaction to gadolinium * Patients with history of seizure * Renal insufficiency (eGFR of \< 45ml/min/1.73m2 using the MDRD equation) * Pregnant or breastfeeding women
Assessing the Response Rate of Neo-adjuvant Taxotere and Trastuzumab in Nigerian Women With Breast Cancer
NCT03879577
Active, positions filled
Conditions Breast Cancer, Breast Cancer Female, HER...
Phase PHASE2
Enrollment 53
Locations 1 sites
Compensation Phase 2: Typically $500-$2,000
Data Updated 2026-07-29
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Study Details Design, interventions, and primary outcomes

About This Study

This is a one stage phase II study with a single arm design. It will be conducted in HER-2 positive breast cancer patients in Nigeria who are chemotherapy/hormonal treatment naive.

Design

Study type: Interventional Phases: Phase2 Allocation: Intervention model: Single Group Primary purpose: Treatment Masking/blinding: None

Interventions / Regimen

  • Drug: Docetaxel — Administered to all patients for a minimum of 4 cycles for 12 weeks.
  • Drug: Herceptin — Administered for 18 cycles every three weeks (52 weeks) for each patient starting at the first day of treatment with docetaxel.
  • Drug: FEC — Only administered to patients who received docetaxel and herceptin and were assessed as having poor response (defined as stable disease or progressive disease or partial response inoperable).
  • Drug: Tamoxifen — Only administered to hormone-receptor positive patients. Patients will receive tamoxifen or letrozole.
  • Drug: Letrozole — Only administered to hormone-receptor positive patients. Patients will receive tamoxifen or letrozole.
  • Drug: LHRH agonist — Administered to all premenopausal patients.

Primary Outcomes

  • Number of Participants With Complete Pathologic Response (pCR) (4-6 months)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE2
Status: Active, positions filled
Start Date: 2019-11-25
Completion: 2026-09-30
Eligibility
Age: 18 Years
Sex: FEMALE
Volunteers: false
Enrollment: 53 (ACTUAL)
Sponsor & Investigators
Lead Sponsor: University of Chicago
Principal Investigators:
  • Olufunmilayo I Olopade, MD (PRINCIPAL_INVESTIGATOR) - University of Chicago
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Drug: Docetaxel — Administered to all patients for a minimum of 4 cycles for 12 weeks.
  • Drug: Herceptin — Administered for 18 cycles every three weeks (52 weeks) for each patient starting at the first day of treatment with docetaxel.
  • Drug: FEC — Only administered to patients who received docetaxel and herceptin and were assessed as having poor response (defined as stable disease or progressive disease or partial response inoperable).
  • Drug: Tamoxifen — Only administered to hormone-receptor positive patients. Patients will receive tamoxifen or letrozole.
  • Drug: Letrozole — Only administered to hormone-receptor positive patients. Patients will receive tamoxifen or letrozole.
Study Locations (1 sites)
University College Hospital, Ibadan, Nigeria, Ibadan, Nigeria
Eligibility Criteria
Inclusion Criteria: 1. Women ages of 18 to 70 years old 2. Biopsy-accessible breast tumor of significant size for core needle biopsy/ultrasound measurable (≥ 2cm) 3. Patients with histologically confirmed carcinoma of the female breast with 3+ positive HER2 status by IHC 4. Clinical stages IIA -IIIC (AJCC 2009) 5. Chemotherapy-naïve patients (for this malignancy) 6. Performance status: ECOG performance status 0-1 (Appendix A) 7. Non-pregnant and not nursing. Women of childbearing potential must take the pregnancy test and must commit to receive LHRH agonist Zoladex (goserelin) for two years starting from the commencement of the study medications 8. Required Initial Laboratory Data. Adequate hematologic, renal and hepatic function, as defined by each of the following: 1\. Granulocyte ≥ 1,500/μL 2. Platelet count ≥ 100,000/μL 3. Absolute neutrophil count (ANC) ≥ l500/μL 4. Hemoglobin ≥ 10g/dL 5. Bilirubin ≤ 1.5 x upper limit of normal 6. SGOT and SGPT \< 2.5 x upper limit of normal 7. Creatinine within institutional normal limits or glomerular filtration rate ≥ 30 mL/min/1.73 m2 by CKD EPI equation (see http://mdrd.com/ for calculator) 9\. ECHO: Baseline left ventricular ejection fraction of ≥ 55% Exclusion Criteria: 1. Pregnant or lactating women. Women of childbearing potential not using a reliable and appropriate contraceptive method. Postmenopausal women must have been amenorrheic for at least 12 months to be considered of non-childbearing potential. Patients of childbearing potential will agree to continue the use of acceptable form of contraception for 24 months from the date of last Herceptin administration. 2. Patients with distant metastasis (brain and/or visceral metastasis) 3. Serious, uncontrolled, concurrent infection(s). 4. Treatment for other carcinomas within the last 5 years, except non-melanoma skin cancer and treated cervical carcinoma in-situ (CCIS) 5. Participation in any investigational drug study within 4 weeks preceding the start of study treatment 6. Other serious uncontrolled medical conditions that the investigator feels might compromise study participation including but not limited to chronic or active infection, HIV-positive patient, uncontrolled hypertension, symptomatic congestive heart failure, unstable angina pectoris, uncontrolled Diabetes mellitus, or psychiatric illness/social situations that would limit compliance with study requirements. 7. Patients with HER2-negative disease
Study Of Entrectinib (Rxdx-101) in Children and Adolescents With Locally Advanced Or Metastatic Solid Or Primary CNS Tumors And/Or Who Have No Satisfactory Treatment Options
NCT02650401
Active, positions filled
Conditions Solid Tumors, CNS Tumors
Phase PHASE1, PHASE2
Enrollment 69
Locations 26 sites
Compensation Phase 1: Typically $1,000-$5,000
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

This is an open-label, Phase 1/2 multicenter dose escalation study in pediatric patients with relapsed or refractory extracranial solid tumors (Phase 1), with additional expansion cohorts (Phase 2) in patients with primary brain tumors harboring NTRK1/2/3 or ROS1 gene fusions, and extracranial solid tumors harboring NTRK1/2/3 or ROS1 gene fusions.

Design

Study type: Interventional Phases: Phase1, Phase2 Allocation: Non Randomized Intervention model: Single Group Primary purpose: Treatment Masking/blinding: None

Interventions / Regimen

  • Drug: Entrectinib — TRKA/B/C, ROS1, and ALK inhibitor

Primary Outcomes

  • Maximum Tolerated Dose (MTD) (Approximately 6 months)
  • Recommended Phase 2 Dose (RP2D) of F1 Formulation In Pediatric Participants Able To Swallow Intact Capsules (Approximately 6 months)
  • Recommended Phase 2 Dose (RP2D) of F06 Formulation In Pediatric Participants Able To Swallow Intact Capsules (Approximately 6 months)
  • Recommended Phase 2 Dose (RP2D) of F06 Formulation In Pediatric In Participants Dosed Via Feeding Tube (Nasogastric Tube Or Gastric Tube) (Approximately 6 months)
  • Recommended Phase 2 Dose (RP2D) Of Minitablets/F15 Formulation In Pediatric Participants Unable To Swallow Intact Capsules (Approximately 6 months)
  • Cohort B: Objective Response Rate (ORR) (Approximately 6 months)
  • Cohort D: ORR (Approximately 6 months)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE1, PHASE2
Status: Active, positions filled
Start Date: 2016-05-03
Completion: 2026-06-30
Eligibility
Age: 0 Years
Sex: ALL
Volunteers: false
Enrollment: 69 (ACTUAL)
Sponsor & Investigators
Lead Sponsor: Hoffmann-La Roche
Principal Investigators:
  • Clinical Trials (STUDY_DIRECTOR) - Hoffmann-La Roche
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Drug: Entrectinib — TRKA/B/C, ROS1, and ALK inhibitor
Study Locations (26 sites)
University of California San Diego, La Jolla, California 92093-0706 United States
UCSF Benioff Children's Hospital, San Francisco, California 94158 United States
Children's Hospital Colorado, Aurora, Colorado 80045 United States
Egleston Children's Hospital at Emory University Atlanta, Atlanta, Georgia 30322 United States
University of Chicago, Chicago, Illinois 60637 United States
Johns Hopkins University, Baltimore, Maryland 21205 United States
Dana Farber Cancer Institute, Boston, Massachusetts 02215 United States
Washington University,St. Louis Children's Hospital, St Louis, Missouri 63110 United States
Memorial Sloan Kettering Cancer Center, New York, New York 10065 United States
Nationwide Children's Hospital, Columbus, Ohio 43205 United States
Eligibility Criteria
Inclusion Criteria: 1. Disease status: * Phase 1 portion (closed): Participants must have measurable or evaluable disease, as defined by RECIST v1.1 * Phase 2 portion: * Part B: Participants must have measurable or evaluable disease, as defined by RANO * Part C (closed): Participants must have measurable or evaluable disease, as defined by RECIST v1.1 ± Curie Scale * Part D: Participants must have measurable or evaluable disease, as defined by RECIST v1.1 * Part E (closed): Participants must have measurable or evaluable disease, as defined by RECIST v1.1 ± Curie Scale or RANO 2. Tumor type: * Phase 1 portion: \* Part A: Relapsed or refractory extracranial solid tumors * Phase 2 portion * Part B: Primary brain tumors with NTRK1/2/3 or ROS1 gene fusions; gene fusions are defined as those predicted to translate into a fusion protein with a functional TRKA/B/C or ROS1 kinase domain, without a concomitant second oncodriver as determined by a nucleic acid-based diagnostic testing method * Part D: Extracranial solid tumors (including NB) with NTRK1/2/3 or ROS1 gene fusions; gene fusions are defined as those predicted to translate into a fusion protein with a functional TRKA/B/C or ROS1 kinase domain, without a concomitant second oncodriver as determined by a nucleic acid-based diagnostic testing method 3. Histologic/molecular diagnosis of malignancy at diagnosis or the time of relapse 4. Archival tumor tissue from diagnosis or, preferably, at relapse 5. Performance status: Lansky or Karnofsky score ≥ 60% and minimum life expectancy of at least 4 weeks 6. Prior therapy: Participants must have a disease that is locally advanced, metastatic, or where surgical resection is likely to result in severe morbidity, and who have no satisfactory treatment options for solid tumors and primary CNS tumors that are neurotrophic tyrosine receptor kinase (NTRK) or ROS1 fusion-positive 7. Participants must have recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to enrollment 8. Adequate organ and neurologic function 9. Females of childbearing potential must have a negative serum pregnancy test during screening and be neither breastfeeding nor intending to become pregnant during study participation. Agreement to remain abstinent or use use combined contraceptive methods prior to study entry, for the duration of study participation and in the following 90 days after discontinuation of study treatment. 10. For male participants with a female partner of childbearing potential or a pregnant female partner: Agreement to remain abstinent or use a condom during the treatment period and for at least 3 months after the last dose of study drug Exclusion Criteria: 1. Receiving other experimental therapy 2. Known congenital long QT syndrome 3. History of recent (3 months) symptomatic congestive heart failure or ejection fraction ≤50% at screening 4. Known active infections 5. Familial or personal history of congenital bone disorders, bone metabolism alterations or osteopenia 6. Receiving Enzyme Inducing Antiepileptic Drugs (EIAEDs) within 14 days of first dose. 7. Prior treatment with approved or investigational TRK or ROS1 inhibitors 8. Known hypersensitivity to entrectinib or any of the other excipients of the investigational medicinal product 9. Patients with NB with bone marrow space-only disease 10. Incomplete recovery from acute effects of any surgery prior to treatment. 11. Active gastrointestinal disease or other malabsorption syndromes that would impact drug absorption. 12. Other severe acute or chronic medical or psychiatric condition or lab abnormality that may increase the risk associated with study participation, drug administration or may interfere with the interpretation of study results.
Mediterranean Diet and Inequality in Early Breast Cancer
NCT07007169
Recruiting
Conditions Early Breast Cancer
Phase PHASE2
Enrollment 105
Locations 2 sites
Compensation Phase 2: Typically $500-$2,000
Data Updated 2026-07-29
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Study Details Design, interventions, and primary outcomes

About This Study

Social determinants such as education, income, marital status, and social networks play a crucial role in cancer outcomes, including breast cancer. One potential influencing factor is diet, and the Mediterranean diet has been shown to benefit both the health and the microbiome. This raises the question: Does adherence to the Mediterranean diet impact the microbiome, quality of life, overall well-being, and outcomes in breast cancer patients undergoing (neo)adjuvant treatment, particularly among those with unfavorable socioeconomic determinants? The Mediterranean diet consists of plant foods such as vegetables, fruits, nuts, seeds, berries, legumes, herbs, and spices. It also features animal proteins like fish, meat, and cheese, along with fat from olive oil. Thus, adherence to the Mediterranean diet is adherence to the official Danish diet recommendations. This phase II clinical trial is an interdisciplinary study combining nutrition, sociology, and health research. Breast cancer patients candidates for (neo)adjuvant treatment at four oncology departments in Region South Denmark will be randomized 2:1 to the Mediterranean diet (with individual dietary guidance from a nutrition therapist aiming at daily consumption of a minimum of 30 grams of dietary fiber and weekly consumption of a minimum of 30 different plant foods; minimizing the amount of ultra-processed food) versus the patient's regular diet, in conjuction with the (neo)adjuvant chemotherapy. The trial's primary endpoint will be changes in gut microbiota composition in feces. The study evaluates how the Mediterranean diet affects the microbiota (evaluated using Oxford Nanopore Technology 16S sequencing on fecal samples); short-chain fatty acids in stool and plasma (assessed by mass spectrometry); immune system (using flow cytometry for immune cell determination in blood and immunohistochemical determination of immune cells in the tumor tissue); and patients' social quality of life, overall well-being, sense of empowerment, and personal feeling of agency (using the WHOQOL-100 questionnaire); taking into account the impact of the distance from the patient residence to the hospital (tracked from GEOTEAM at Statistics Denmark), and socioeconomic factors (using the DREAM database). The evaluation of biological parameters is based on the suggested mechanism of action. A diet rich in various plant foods and dietary fiber will alter the gut microbiota, promoting bacteria producing high amounts of short-chain fatty acids. These fatty acids will activate immune cells, aiding in the destruction of cancer cells. The study will also assess whether the Mediterranean diet will positively impact the patients' social quality of life, overall well-being, sense of empowerment, and personal feeling of agency. The Mediterranean diet may not only lead to improved dietary habits but also serve as a crucial tool for breast cancer patients, particularly among those with unfavorable socioeconomic…

Design

Study type: Interventional Phases: Phase2 Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: None

Interventions / Regimen

  • Dietary Supplement: The goal is daily consumption of a minimum of 30 grams of dietary fiber and weekly consumption of a minimum of 30 different plant foods; minimizing the amount of ultra-processed food. — The intervention group will receive personalized education and guidance from a nutrition therapist.
  • Other: Standard Diet — The control group will continue their normal diet, and not receive guidance or participate in group sessions.

Primary Outcomes

  • Change in microbiota composition (Baseline to Day 1 of chemotherapy cycle 6. Each cycle is 3 weeks for regular schedule or 2 weeks for accelerated schedule, as per clinician decision.)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE2
Status: Recruiting
Start Date: 2025-03-27
Completion: 2036-03
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: true
Enrollment: 105 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Esbjerg Hospital - University Hospital of Southern Denmark
Collaborators: Vejle Hospital, Hospital of Southern Jutland, Odense University Hospital, Syddansk Universitet, Denmark, University of Copenhagen, Aarhus University Hospital, Danish Breast Cancer Cooperative Group, Aalborg University
Contact Information
Study Contact:
Frede Donskov, Clinical Professor, MD, DMSc,
+45 2053 3235
fdonskov@health.sdu.dk
Lone Gamrath, PhD Fellow
+45 2920 3221
Lone.Gamrath@rsyd.dk
Interventions
  • Dietary Supplement: The goal is daily consumption of a minimum of 30 grams of dietary fiber and weekly consumption of a minimum of 30 different plant foods; minimizing the amount of ultra-processed food. — The intervention group will receive personalized education and guidance from a nutrition therapist.
  • Other: Standard Diet — The control group will continue their normal diet, and not receive guidance or participate in group sessions.
Study Locations (2 sites)
University Hospital of Southern Denmark, Esbjerg, Esbjerg, 6700 Denmark
Sygehus Lillebaelt, Vejle, Vejle, 7100 Denmark
Eligibility Criteria
Inclusion Criteria: 1. Signed written informed consent approved by the Ethical Review Board. 2. Age ≥ 18 3. Histologically confirmed unilateral adenocarcinoma of the breast, stage I-III, candidates for neoadjuvant chemotherapy followed by curative surgery, or adjuvant chemotherapy after curative surgery, according to the Danish Breast Cancer Group guidelines 48. The addition of trastuzumab and pertuzumab in HER2-positive tumors, or pembrolizumab in triple-negative tumors, per Danish Breast Cancer Group guidelines 48, is allowed as an adjunct to chemotherapy. 4. Good performance status (WHO performance status 0 or 1). 5. Willingness by the patient to undergo treatment and study-related procedures according to the protocol. 6. Have a smartphone or computer to which it is possible to receive emails (for food diary; www.myfood24.org) 7. Must be willing to restrict from probiotic (living microorganisms) supplements during the study. Fermented foods are allowed. \- Exclusion Criteria: 1. Clinical or radiological signs of metastatic disease. 2. History of other malignancy within the last 5 years, except for carcinoma in situ of the cervix or non-melanoma skin cancer. 3. Previous chemotherapy for cancer or other malignant disease. 4. Major altered digestive system disorders (e.g. gastric by-pass or Crohn's disease or ulcerative colitis) 5. Unable to communicate effectively in Danish or English.
Effect of Huaier Granule on Adjuvant Treatment for High-risk Early-stage Triple-negative Breast Cancer
NCT04790305
Recruiting
Conditions Carcinoma Breast, Triple-negative Breast...
Phase PHASE4
Enrollment 1072
Locations 34 sites
Compensation Phase 4: Typically $100-$500
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

This is a prospective, multicenter, randomized, parallel controlled, open-label study. The primary purpose of this study is to evaluate the efficacy of Huaier Granule on postoperative adjuvant therapy of high-risk early-stage triple-negative invasive ductal carcinoma. The Secondary purposes are to evaluate the safety of long-term use of Huaier granules as postoperative adjuvant treatment of high-risk early-stage triple-negative invasive ductal carcinoma, and the changes of quality of life score after treatment with Huaier granule.

Design

Study type: Interventional Phases: Phase4 Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: None

Interventions / Regimen

  • Drug: Huaier Granule — The subjects in the experimental group will be treated with Huaier Granule continuously for 2 years or until the disease progressed, intolerable toxicity, withdrawal of informed consent form or died for any reason.

Primary Outcomes

  • 3-year rates of disease-free survival (Start of treatment until 3-year follow-up)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE4
Status: Recruiting
Start Date: 2021-06-18
Completion: 2028-07-28
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 1072 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Fudan University
Collaborators: LinkDoc Technology (Beijing) Co. Ltd., Huazhong University of Science and Technology
Principal Investigators:
  • Zhimin Shao, PhD (PRINCIPAL_INVESTIGATOR) - Fudan University
Contact Information
Study Contact:
Zhimin Shao, PhD
+86-18017312288
zhimingshao@yahoo.com
Liang Huang, PhD
+86-18121299334
fdhlyx@163.com
Interventions
  • Drug: Huaier Granule — The subjects in the experimental group will be treated with Huaier Granule continuously for 2 years or until the disease progressed, intolerable toxicity, withdrawal of informed consent form or died for any reason.
Study Locations (34 sites)
The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui China
The First Affiliated Hospital of USTC, Anhui Provincial Hospital, Hefei, Anhui China
Cancer Hospital Chinese Academy of Medical Science, Beijing, Beijing Municipality China
The Second Affiliated Hospital of Chongqing Medical University, Chongqing, Chongqing Municipality China
Fujian Cancer Hospital, Fuzhou, Fujian China
Guangdong Provincial Hospital of Traditional Chinese Medicine, Guangzhou, Guangdong China
Guangdong Provincial People's Hospital, Guangzhou, Guangdong China
The Fourth Hospital of Hebei Medical University, Hebei Tumor Hospital, Shijiazhuang, Hebei China
The First Affiliates Hospital of Ha'erbin University, Harbin, Heilongjiang China
Henan Provincial People's Hospital, Zhengzhou, Henan China
Eligibility Criteria
Inclusion Criteria: 1. Aged from 18 to 70. 2. Histologically confirmed as breast invasive ductal carcinoma. 3. Molecular typing of breast lesions is triple-negative breast cancer, when the patient had multicentric lesions at the same time, all invasive lesions were confirmed as triple-negative. 4. Regional lymph node metastasis confirmed by postoperative pathology \[except isolated tumor cells ( ITC )\], or tumor response did not achieve pathological complete response (pCR) after neoadjuvant therapy \[neoadjuvant chemotherapy completed at least four cycles, the breast has residual invasive cancer or axillary lymph node metastasis ( except isolated tumor cells ) .\] 5. There was no local recurrence and distant metastasis of the tumor. 6. The time of randomization is during the postoperative adjuvant therapy or within 60 days after the end of the last postoperative adjuvant therapy. 7. Eastern Cooperative Oncology Group performance status (ECOG PS) ≤ 1. 8. Hepatic function and renal function: serum creatinine level ≤ 1.5 × upper limit of normal (ULN), aspartate aminotransferase (AST) concentration / alanine aminotransferase (ALT) concentration≤ 2.5 × ULN,total serum bilirubin concentration≤ 1.5 × ULN. 9. Blood routine: neutrophil count ≥ 1.5\*109 / L, platelet count ≥ 100\*109 / L, hemoglobin concentration ≥ 90 g / L (without transfusion). 10. The participants volunteered to join the study with good compliance and signed an informed consent form. Exclusion Criteria: 1. Bilateral breast cancer. 2. Complicated with severe cardiopathy, hepatopathy, nephropathy, endocrine system diseases. According to the researchers' judgement, the comorbidities can cause unacceptable safety risks and affect participants' compliance with research programs. 3. Suffering from malignant tumors other than breast cancer (except cured basal cell carcinoma of the skin and carcinoma in situ of the cervix) in the past 5 years. 4. Allergic to Huaier granule. 5. Pregnant or lactating women, and those who planning a pregnancy during the study period. 6. Participating in other clinical trials or participated in other clinical studies within 3 months. 7. Patients with a poor compliance, or they are not appropriate for this study because of other reasons considered by the researchers.
A Quasi-Experimental Study to Improve Breast Cancer Awareness Among University Students
NCT07118969
Active, positions filled
Conditions Breast Cancer Awareness, Health Educatio...
Phase Not Applicable
Enrollment 100
Locations 1 sites
Compensation Compensation varies
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

Breast cancer is one of the most common cancers among women worldwide and a leading cause of cancer-related deaths. Despite advances in early detection and screening methods, breast cancer remains a significant public health issue, especially in populations with low awareness levels. This study aims to evaluate the effect of a breast cancer education program on the knowledge and awareness of female students at Mardin Artuklu University. The study will include 100 voluntary female students aged 18 and older from five faculties, selected using cluster sampling. Participants will complete a Personal Information Form, the Comprehensive Breast Cancer Knowledge Test, and the Breast Cancer Awareness Scale before the intervention. They will then attend a five-session breast cancer education program, with each session lasting 90 minutes. A post-test will be administered two months after the completion of the training. The education program is expected to improve students' knowledge and awareness of breast cancer, encourage early detection behaviors, and contribute to the prevention and early diagnosis of breast cancer.

Design

Study type: Observational Observational model: Cohort Time perspective: Prospective

Interventions / Regimen

  • Other: Breast Cancer Awareness Training — A structured breast cancer education program consisting of five sessions, each lasting 90 minutes. The program covers breast cancer risk factors, early detection methods including breast self-examination (BSE), clinical breast examination, mammography, and health-promoting behaviors. The sessions are conducted in group settings within university faculties. The education aims to increase participants' knowledge and awareness of breast cancer and encourage early detection practices.

Primary Outcomes

  • Change in Breast Cancer Knowledge (Baseline and 2 months post-intervention)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: OBSERVATIONAL
Phase: Not Applicable
Status: Active, positions filled
Start Date: 2025-04-08
Completion: 2026-04-08
Eligibility
Age: 18 Months
Sex: FEMALE
Volunteers: true
Enrollment: 100 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Mardin Artuklu University
Collaborators: The Scientific and Technological Research Council of Turkey
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Other: Breast Cancer Awareness Training — A structured breast cancer education program consisting of five sessions, each lasting 90 minutes. The program covers breast cancer risk factors, early detection methods including breast self-examination (BSE), clinical breast examination, mammography, and health-promoting behaviors. The sessions are conducted in group settings within university faculties. The education aims to increase participants' knowledge and awareness of breast cancer and encourage early detection practices.
Study Locations (1 sites)
Mardin Artuklu Unıversity, Mardin, Artuklu 47100 Turkey (Türkiye)
Eligibility Criteria
Inclusion Criteria: * Participants must be students at Mardin Artuklu University. Exclusion Criteria: * Students with any physical or mental health issues * Individuals with a diagnosis or history of mental illness will be excluded from the study.
S1501 Dual Observational and Randomized Cohort Study of Patients With Metastatic HER-2+ Breast Cancer at Risk of Cardiac Toxicity
NCT03418961
Recruiting
Conditions Cardiotoxicity, HER2/Neu Positive, Metas...
Phase PHASE3
Enrollment 491
Locations 590 sites
Compensation Phase 3: Typically $200-$1,000
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

This trial has two cohorts of patients with human epidermal growth factor receptor (HER)-2-positive breast cancer that has spread to other places in the body. All patients must be receiving trastuzumab-based treatment. Both cohorts are being observed for cardiac toxicity. The largest cohort (currently open to accrual) is observational, and contains patients who are taking a beta blocker, ACE inhibitor, or ARB as well as their trastuzumab-based treatment. The goal is to understand how common cardiac problems are in this group of patients at high risk. The smaller cohort (currently closed to accrual) is randomized. Patients in this second cohort are randomized to either carvedilol or no treatment, with the goal of seeing whether carvedilol (used to treat heart failure and high blood pressure) may prevent the heart from side effects of chemotherapy.

Design

Study type: Interventional Phases: Phase3 Allocation: Randomized Intervention model: Parallel Primary purpose: Supportive Care Masking/blinding: Single

Interventions / Regimen

  • Drug: Carvedilol — Given PO
  • Other: Laboratory Biomarker Analysis — Correlative studies
  • Other: Patient Observation — Undergo observation

Primary Outcomes

  • Time to the first identification of cardiac dysfunction (Up to 108 weeks)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE3
Status: Recruiting
Start Date: 2017-11-01
Completion: 2027-09-15
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 491 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: SWOG Cancer Research Network
Collaborators: National Cancer Institute (NCI)
Principal Investigators:
  • Justin Floyd (PRINCIPAL_INVESTIGATOR) - SWOG Cancer Research Network
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Drug: Carvedilol — Given PO
  • Other: Laboratory Biomarker Analysis — Correlative studies
  • Other: Patient Observation — Undergo observation
Study Locations (590 sites)
Anchorage Associates in Radiation Medicine, Anchorage, Alaska 98508 United States
Alaska Breast Care and Surgery LLC, Anchorage, Alaska 99508 United States
Alaska Oncology and Hematology LLC, Anchorage, Alaska 99508 United States
Alaska Women's Cancer Care, Anchorage, Alaska 99508 United States
Anchorage Oncology Centre, Anchorage, Alaska 99508 United States
Katmai Oncology Group, Anchorage, Alaska 99508 United States
Providence Alaska Medical Center, Anchorage, Alaska 99508 United States
Fairbanks Memorial Hospital, Fairbanks, Alaska 99701 United States
CHI Saint Vincent Cancer Center Hot Springs, Hot Springs, Arkansas 71913 United States
Kaiser Permanente-Deer Valley Medical Center, Antioch, California 94531 United States
Eligibility Criteria
Inclusion Criteria: * STEP 1 REGISTRATION Patients must: 1. Have metastatic breast cancer, AND 2. Be initiating within 11 calendar days of Step 1 Registration OR be continuing trastuzumab-based HER-2 targeted therapy without concurrent anthracyclines, AND 3. Be receiving the trastuzumab-based HER-2 targeted therapy for metastatic disease in first, second, third-, or fourth-line setting. Patients may have brain metastasis. There is no limit for number of doses of HER-2 targeted therapy prior to registration. Examples of eligible HER-2 targeted therapy: * Trastuzumab or a trastuzumab biosimilar * Trastuzumab + chemotherapy or hormonal therapy * Trastuzumab + other HER-2 targeted agent with or without chemotherapy (such as pertuzumab, lapatinib, and tucatinib) * Ado-trastuzumab (Kadcyla®) * Fam-trastuzumab deruxtecan (Enhertu) NOTE: Patients on lapatinib without trastuzumab are not eligible. Planned treatment with concurrent HER-2 targeted therapy and anthracyclines is not permitted. * Patients must be at increased risk for cardiotoxicity defined by at least one of the following: 1. Previous anthracycline exposure OR 2. 1 or more of the following risk factors for heart disease: * LVEF 50-54% by local ECHO read\* * Age ≥ 65 * BMI ≥ 30 kg/m2 * Current or prior anti-hypertensive therapy * Diagnosis of coronary artery disease (CAD) * Diagnosis of diabetes mellitus * Diagnosis of atrial fibrillation/flutter Note: ECHO can be performed at any time prior to registration with the most recent being sent. * Patients must not have taken within 21 days prior to Step 1 Registration, be currently taking at the time of Step 1 Registration or planning to take once registered to Step 1 a beta blocker, ARB, or ACE inhibitor, in order to be randomized (Arms 1 and 2). Patients enrolling in the observational cohort (Arm 3) must be currently taking a beta blocker, ARB, or ACE inhibitor at the time of Step 1 Registration. * Patients must have a Zubrod Performance status of 0-2 * Patients must have a complete physical examination and medical history within 28 days prior to registration * Patients must have LVEF \>= 50% echocardiogram (2D or 3D) within 28 days prior to registration. The echocardiogram must be obtained from a S1501 validated ECHO laboratory (lab) and submitted for central review by the S1501 ECHO core lab. If a 3D echocardiogram is performed at baseline, sites must ensure that standard 2D images, including 40chamber and 2-chamber views, are also obtained and submitted at subsequent timepoints. All follow-up echocardiograms (every 12 weeks) must be performed using 2D imaging to allow for standardized assessments. Follow-up scans must be completed at a site that can provide 2D images per protocol requirements. The echocardiograms cannot be submitted for central read until after Step 1 registration is complete. * Patients must have adequate hepatic function as evidenced by all of the following within 28 days prior to registration: * Serum bilirubin \< 3.0 x institutional upper limit of normal (IULN) * Serum glutamic oxaloacetic transaminase (SGOT)/aspartate aminotransferase (AST) and serum glutamic pyruvic transaminase (SGPT)/alanine aminotransferase (ALT) \< 5.0 x IULN * Patients must not be dialysis dependent * No other prior malignancy is allowed except for the following: adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, prostate cancer on active surveillance, adequately treated stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease free for five years * Patients must not be pregnant or nursing due to potential fetal or nursing infant harm; women/men of reproductive potential must have agreed to use an effective contraceptive method, a woman is considered to be of "reproductive potential" if she has had menses at any time in the preceding 12 consecutive months; in addition to routine contraceptive methods, "effective contraception" also includes heterosexual celibacy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) defined as a hysterectomy, bilateral oophorectomy or bilateral tubal ligation; however, if at any point a previously celibate patient chooses to become heterosexually active during the time period for use of contraceptive measures outlined in the protocol, he/she is responsible for beginning contraceptive measures * Patients must be willing to submit blood specimens * Sites must seek additional patient consent for the future use of specimens * Patients must be informed of the investigational nature of this study and must sign and give written informed consent in accordance with institutional and federal guidelines * For participants with impaired decision-making capabilities, legally authorized representatives may sign and give informed consent on behalf of study participants in accordance with applicable federal, local, and CIRB regulations. * As a part of the OPEN registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system * STEP 2 REGISTRATION (Randomization) * Patients must not be registered to step 2 until confirming via RAVE EDC that the patient's LVEF by echocardiogram was \>= 50% by central review. Patients must be registered within 21 calendar days of submission of the ECHO study/ * Site must verify that there is no known change in the step 1 eligibility since initial registration
HP-211 Safety and Proof of Concept Dose Ranging Study in Patients With Type 2 Diabetes
NCT07546929
Recruiting
Conditions Type 2 Diabetes
Phase PHASE2
Enrollment 300
Locations 25 sites
Compensation Phase 2: Typically $500-$2,000
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

Blood sugar levels are controlled by insulin, a hormone made by cells in the pancreas. After a meal, carbohydrates are broken down into glucose which is absorbed from the intestine into the blood leading to a rise in glucose (blood sugar) which triggers the secretion of insulin. Insulin binds to cells in several tissues including liver, muscle, and fat, triggering cells to take up glucose and bring the blood glucose level back to normal. A high blood sugar level is known as diabetes. The most common form of diabetes, type 2 diabetes, is caused by insulin resistance; that is, a reduced ability of insulin to stimulate glucose uptake into cells. The body compensates for insulin resistance by making more insulin; type 2 diabetes occurs when the pancreas can no longer make enough insulin to control blood glucose. The high blood glucose and insulin levels lead to long-term complications such as heart attacks, kidney failure, reduced sensation and poor circulation in the feet and legs. High insulin levels also increase the incidence of cancers, stroke, and dementia. Reducing blood glucose levels with oral medications and insulin reduces risk of diabetic complications. There are several types of oral medications available for treating diabetes; however, they do not always control blood glucose adequately. In addition, these drugs have complications and are not used to treat insulin resistance and prediabetes - a condition when blood glucose is higher than normal but not high enough to be classified as diabetes. Prediabetes often progresses to diabetes over a period of months or years. Effective and safe treatments for insulin resistance may prevent the onset of diabetes or even reverse diabetes if diagnosed in its early stages before substantial damage to the pancreas has occurred. HP-211 is a botanical extract whose active ingredients are derived from herbs and vegetables present in normal diets. HP-211 has been shown in laboratory studies in cell culture, in animal studies, and in a previous Phase 1 study to enhance the ability of insulin to stimulate glucose uptake into cells. Thus, HP-211 may reduce the blood glucose and circulating insulin levels of subjects with type 2 diabetes after a meal. HP-211 may also reduce glucose and insulin responses to a greater extent in insulin-resistant as compared to insulin-sensitive subjects. Subjects will take 0, 1, 2 or 3 tablets of HP-211 in the morning and evening for 90 days. Hemoglobin A1c (HbA1c, or "A1c"), a measure of the average amount of glucose present in the blood, will be measured during the trial period.

Design

Study type: Interventional Phases: Phase2 Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: Quadruple

Interventions / Regimen

  • Drug: HP-211 — HP-211 is an investigational botanical extract derived from Cichorium endivia var. latifolium, Lactuca sativa, and Artemisia dracunculus.
  • Drug: Placebo — Matching placebo administered orally twice daily (BID).

Primary Outcomes

  • Change from Baseline in Hemoglobin A1c (HbA1c) (After 12 weeks of treatment.)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE2
Status: Recruiting
Start Date: 2023-02-03
Completion: 2026-10
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 300 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Housey Healthcare ULC
Contact Information
Study Contact:
Housey Study Info
(248) 663-7000
StudyInfo@housey.com
Interventions
  • Drug: HP-211 — HP-211 is an investigational botanical extract derived from Cichorium endivia var. latifolium, Lactuca sativa, and Artemisia dracunculus.
  • Drug: Placebo — Matching placebo administered orally twice daily (BID).
Study Locations (25 sites)
Alliance Clinical Canoga Park (Hope Clinical Research), Canoga Park, California 91303 United States
Universal Axon Clinical Research, Doral, Florida 33166 United States
Velocity Clinical Research New Smyrna Beach, Edgewater, Florida 32132 United States
Southwest General Healthcare Center, Fort Myers, Florida 33907 United States
Avantis Clinical Research, Miami, Florida 33155 United States
IMIC Research, Miami, Florida 33176 United States
South Broward Research, Miramar, Florida 33027 United States
David Kavtaradze MD InC, Cordele, Georgia 31015 United States
AMR Clinical - El Dorado, El Dorado, Kansas 67042 United States
Tandem Clinical Research (Interspond), Marrero, Louisiana 70072 United States
Eligibility Criteria
Key Inclusion Criteria: * Have type 2 diabetes for greater than 3 months and no longer than 5 years by history prior to entering the trial, based upon ADA disease diagnostic criteria. * Have an HbA1c \> 6.5% and ≤ 10% as determined by the central lab at Visit 1 (Screening). * Have been on a stable maximum dose of metformin for at least 3 months prior to entering the study or have been on stable therapy of diet and exercise only for at least 3 months. Stable treatment is defined as no change in treatment or dose in the last 3 months. Key Exclusion Criteria: * Have known type 1 diabetes. * Diabetic complications * Have taken any oral (other than metformin) or injectable treatment (insulin or GLP-1 RA classes or other) for type 2 diabetes currently or for greater than a 4 week duration previously. Previous treatment must have been stopped at least 3 months prior to screening * Systolic blood pressure greater than 150 mmHg or a diastolic blood pressure greater than 100 mmHg at Visit 1 on average after three supine measurements, or a known history of renal artery stenosis. * At baseline, the QT interval corrected by Fridericia (QTcF) ECG findings (\>450 msec for males and \>470 msec for females), left bundle branch block, or cardiac arrhythmia requiring medical or surgical treatment within 6 months prior to Visit 1 on the ECG.
The Effect of Motivational Interviewing on Diabetes Self-Management in Diabetic Patients
NCT06727123
Not yet recruiting
Conditions Diabetes Mellitus
Phase NA
Enrollment 80
Locations 1 sites
Compensation Compensation typically provided
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

Diabetes is a chronic metabolic disorder characterized by high blood sugar due to problems with insulin production or function. Its prevalence has increased significantly in recent decades due to sedentary lifestyles, unhealthy diets, and increasing obesity rates. Type 2 diabetes, in particular, is a major global and national health problem with projections showing that it continues to grow. Effective diabetes management requires patients to adopt healthy behaviors such as following a diet plan, monitoring blood sugar, increasing physical activity, and avoiding risky habits such as smoking. Inadequate adherence to treatment can lead to serious complications such as cardiovascular disease and kidney damage, which can be a burden to patients, families, and healthcare systems. Motivational interviewing, a patient-centered approach, helps individuals overcome resistance to behavioral change. This study was designed experimentally to determine the effect of motivational interviewing on diabetes self-management in patients with type 2 diabetes.

Design

Study type: Interventional Phases: Allocation: Randomized Intervention model: Parallel Primary purpose: Prevention Masking/blinding: None

Interventions / Regimen

  • Other: motivational interviewing — Motivational interviews will be conducted with diabetic patients for 6 months. Patients will be trained before starting the interviews.
  • Other: Control — No application will be made. Routine follow-ups will be made.

Primary Outcomes

  • Diabetes Self-Management (6 months)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: NA
Status: Not yet recruiting
Start Date: 2024-12-20
Completion: 2026-06-20
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: true
Enrollment: 80 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: University of Beykent
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Other: motivational interviewing — Motivational interviews will be conducted with diabetic patients for 6 months. Patients will be trained before starting the interviews.
  • Other: Control — No application will be made. Routine follow-ups will be made.
Study Locations (1 sites)
Istanbul Beykent University, Istanbul, Turkey (Türkiye)
Eligibility Criteria
Inclusion Criteria: * Individuals who agree to participate in the study voluntarily, can speak and understand Turkish, can communicate comfortably, have no hearing, comprehension or vision problems, are literate, use a smartphone, have Type 2 Diabetes and have HbA1c ≥ 7% will be included in the study. Exclusion Criteria: * Patients with cognitive dysfunction and those using antipsychotic medication will not be included.
Multimodal Training Effects in Middle-Aged and Older Adults With Diabetic Sarcopenia
NCT07398495
Recruiting
Conditions Type 2 Diabetes Mellitus (T2DM), Sarcope...
Phase NA
Enrollment 128
Locations 1 sites
Compensation Compensation typically provided
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

This study aims to investigate the effects of a 12-week multimodal exercise intervention on middle-aged and older adults (aged 45\~85 years) with Type 2 Diabetes Mellitus (T2DM). The program combines supervised training, home-based sessions, and digital support to improve muscle function, physical performance, metabolic control, and quality of life.

Design

Study type: Interventional Phases: Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: Single

Interventions / Regimen

  • Behavioral: Multimodal Exercise Program — Participants will engage in a 12-week multimodal exercise program comprising supervised training sessions, home-based exercises, and digital support. To facilitate adherence and proper technique, participants will also receive a "Diabetes and Muscle Health Handbook" as a training guide.

Primary Outcomes

  • Physical Function (5TSTS) (Change from Baseline at Week 12 and Week 24)
  • Handgrip Strength (HGS) (Change from Baseline at Week 12 and Week 24)
  • Skeletal Muscle Mass Index (SMI) (Change from Baseline at Week 12 and Week 24)
  • Sarcopenia Risk: Assessed using the Strength, Assistance with walking, Rise from a chair, Climb stairs, and Falls (SARC-F) questionnaire combined with calf circumference measurement (SARC-CalF). (Change from Baseline at Week 12 and Week 24)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: NA
Status: Recruiting
Start Date: 2026-02-23
Completion: 2026-08-15
Eligibility
Age: 45 Years
Sex: ALL
Volunteers: false
Enrollment: 128 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: yueh chu wu
Contact Information
Study Contact:
yueh chu wu WU YUEH CHU
886-952680613
yueh.chu46240@gmail.com
Interventions
  • Behavioral: Multimodal Exercise Program — Participants will engage in a 12-week multimodal exercise program comprising supervised training sessions, home-based exercises, and digital support. To facilitate adherence and proper technique, participants will also receive a "Diabetes and Muscle Health Handbook" as a training guide.
Study Locations (1 sites)
Chung Shan Medical University Hospital, Taichung, Taiwan 402306 Taiwan
Eligibility Criteria
Inclusion Criteria: * Diagnosed with both Type 2 Diabetes Mellitus (T2DM) and sarcopenia. * Maintained on a stable regimen of oral hypoglycemic agents. * Aged 45 years or older. * Capable of communicating effectively in Mandarin or Taiwanese. * Willing to provide informed consent or have it obtained from a legally authorized representative. Exclusion Criteria: * • Limited limb or joint function that prevents exercise (e.g., recent fractures or dislocations). * Communication barriers or severe emotional/psychological issues (e.g., uncontrolled depression or severe mental illness). * Severe cognitive impairment (e.g., dementia). * End-stage renal disease (ESRD). * Major comorbidities or complications, including active diabetic foot ulcers, amputation, recent myocardial infarction, severe autonomic neuropathy, or a history of stroke within the last 3 years.
Evaluation of Dietary Knowledge and the Habit of Using the Mediterranean Diet in Patients With Diabetes
NCT07431359
Recruiting
Conditions Type 2 Diabetes
Phase Not Applicable
Enrollment 500
Locations 1 sites
Compensation Compensation varies
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

The main aim of this study is to evaluate nutritional knowledge and adherence to the Mediterranean diet through the administration of questionnaires in patients with type 2 Diabetes Mellitus belonging to Outpatient Diabetology Service of the Hospital.

Design

Study type: Observational Observational model: Case Only Time perspective: Prospective

Interventions / Regimen

  • Other: administration of questionnaires - Collection of Clinical Parameters - Hand Grip Test — The acquisition of personal and clinical information and the data obtained from the questionnaires will be carried out in conjunction with the usual control visits planned as part of normal clinical practice

Primary Outcomes

  • Average Nutritional Knowledge Score (NK) (through study completion, an average of 1 year)
  • Mediterranean Diet Adherence (AMD) value (through study completion, an average of 1 year)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: OBSERVATIONAL
Phase: Not Applicable
Status: Recruiting
Start Date: 2025-05-22
Completion: 2026-05-19
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 500 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Casa di Cura Dott. Pederzoli
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Other: administration of questionnaires - Collection of Clinical Parameters - Hand Grip Test — The acquisition of personal and clinical information and the data obtained from the questionnaires will be carried out in conjunction with the usual control visits planned as part of normal clinical practice
Study Locations (1 sites)
Ospedale P. Pederzoli Casa di Cura Privata S.p.A., Peschiera del Garda, Verona 37019 Italy
Eligibility Criteria
Inclusion Criteria: * T2DM in nutritional and/or pharmacological euglycemic treatment (metformin, gliptins, gliflozines, incretin mimetics, pioglitazone) * Signing of informed consent Exclusion Criteria: * Patient with Diabetes Mellitus type 1 * Patients with insulin T2DM treated
CGM Adherence Compared to Finger-stick Glucose Monitoring in Pregnancies With Type 2 Pregestational Diabetes
NCT07184775
Recruiting
Conditions Type 2 Diabetes Mellitus (T2DM), Pregnan...
Phase NA
Enrollment 70
Locations 2 sites
Compensation Compensation typically provided
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

The purpose of this study is to compare patient adherence to blood sugar monitoring during pregnancy using two different measurement methods in pregnancies complicated by pregestational type 2 diabetes (T2DM). Pregnant patients with T2DM are at risk of having larger babies, babies with low sugar levels in the first 24 hours of life, higher rates of cesarean delivery, stillbirth (death of baby inside the womb), and hypertensive or high blood pressure disorders of pregnancy, such as preeclampsia. Prior studies have shown that treating high blood sugars in pregnancy with medications can reduce these risks. To determine the amount of medication needed, recording of blood sugar levels is necessary. This trial aims to determine whether continuous blood sugar monitors have improved patient recording of blood sugar levels over finger stick blood sugar measurements. Patients involved in the study will be assigned to either: 1. Fingerstick glucose monitoring (FSG) 2. Continuous glucose monitoring (CGM) Patients will be randomize in a 1:1 ratio. FSG Group: blood sugar is tested four times daily - once fasting and two hours after every meal (post-prandial). Blood will be tested using a glucometer, and values will be recorded in a blood sugar log from the time of enrollment to the time of delivery. CGM Group: A CGM sensor will be placed on the patient's arm for blood sugar collection every 3-5 minutes. This data is sent to a phone application from the time of enrollment to the time of delivery. These sensors will need to be replaced every 14 days. Percent adherence will be recorded from the time you were randomized to a study group until delivery.

Design

Study type: Interventional Phases: Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: None

Interventions / Regimen

  • Device: Continuous glucose monitor — Continuous glucose monitors are sensors that detect interstitial blood glucose measurements and relay values from their sensor to a receiver (typically a cell phone) to document values every 5 minutes.
  • Device: Glucometer — Glucometer measurement involves a patient performing a finger stick with a lancet to draw blood. They then apply blood to a test strip which is analyzed by a glucometer. The glucose measurement provided by the glucometer is then recorded by the patient in a glucose log.

Primary Outcomes

  • Patient glucose monitoring adherence (through pregnancy episode, typically 20-35 weeks)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: NA
Status: Recruiting
Start Date: 2025-10-01
Completion: 2026-03-01
Eligibility
Age: 18 Years
Sex: FEMALE
Volunteers: false
Enrollment: 70 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Thomas Jefferson University
Collaborators: Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
Contact Information
Study Contact:
Brandy Firman
215-955-8401
brandy.firman@jefferson.edu
Interventions
  • Device: Continuous glucose monitor — Continuous glucose monitors are sensors that detect interstitial blood glucose measurements and relay values from their sensor to a receiver (typically a cell phone) to document values every 5 minutes.
  • Device: Glucometer — Glucometer measurement involves a patient performing a finger stick with a lancet to draw blood. They then apply blood to a test strip which is analyzed by a glucometer. The glucose measurement provided by the glucometer is then recorded by the patient in a glucose log.
Study Locations (2 sites)
Jefferson Health New Jersey, Sewell, New Jersey 08080 United States
Thomas Jefferson University, Philadelphia, Pennsylvania 19107 United States
Eligibility Criteria
Inclusion Criteria: * singleton pregnancies * fetuses without anomalies * diagnosis of Type 2 diabetes * initiation of prenatal care at \<20 weeks gestation Exclusion Criteria: * diagnosis of Type 1 diabetes * allergy to insulin * inability to wear a continuous glucose monitor
Characterization of Cardiovascular Risk Profile and Therapeutic Management in Patients With Type 2 Diabetes Mellitus in Italy
NCT07375069
Recruiting
Conditions Type 2 Diabetes
Phase Not Applicable
Enrollment 3000
Locations 1 sites
Compensation Compensation varies
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

CardioMET is an observational, multicenter, real-life registry, intending to collect data on patients with Type 2 Diabetes Mellitus, attending internal medicine and cardiology outpatient clinics. The aim of the registry is to characterize the cardiovascular risk profile and pharmacological management of Type 2 Diabetes Mellitus in Italy, in accordance with current ESC and AHA guidelines for primary and secondary prevention of CV disease.

Design

Study type: Observational Observational model: Cohort Time perspective: Other

Interventions / Regimen

  • Other: data collection — Data collection on diabetes therapy and follow-up

Primary Outcomes

  • Diabetes treatment adherence according to the most recent European Guidelines (12-24-36-48 months)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: OBSERVATIONAL
Phase: Not Applicable
Status: Recruiting
Start Date: 2022-10-01
Completion: 2027-10-31
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 3000 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Federico II University
Contact Information
Study Contact:
Pasquale Perrone Filardi
+39081/746224
fpperron@unina.it
Interventions
  • Other: data collection — Data collection on diabetes therapy and follow-up
Study Locations (1 sites)
Federico II University of Naples, Department of Advanced Biomedical Sciences, Naples, Napoli 80131 Italy
Eligibility Criteria
Inclusion Criteria: * Age ≥ 18 years; * Diagnosis of type 2 diabetes mellitus (T2DM); * Stable clinical conditions * Outpatient settings * Ability to understand the study procedures and provide written informed consent. Exclusion Criteria: * Patients with type 1 diabetes mellitus; * Active participation in interventional studies; * Any condition that may put the patient at risk by participating in the study.
Efficacy and Safety of HRS9531 in Participants With Type 2 Diabetes Treated With Basal Insulin
NCT07060456
Recruiting
Conditions Type 2 Diabetes
Phase PHASE3
Enrollment 300
Locations 1 sites
Compensation Phase 3: Typically $200-$1,000
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

The study is being conducted to evaluate the efficacy and safety of HRS9531 compared with placebo in participants with type 2 diabetes mellitus not adequately controlled with basal insulin, with or without metformin and/or sodium-glucose cotransporter-2 (SGLT2) inhibitor. The study may include up to 23 visits.

Design

Study type: Interventional Phases: Phase3 Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: Triple

Interventions / Regimen

  • Drug: HRS9531 — HRS9531-low dose
  • Drug: HRS9531 — HRS9531-high dose
  • Drug: Placebo — Placebo

Primary Outcomes

  • Change in HbA1c (from baseline to Week 40)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE3
Status: Recruiting
Start Date: 2025-07-25
Completion: 2027-03
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 300 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Fujian Shengdi Pharmaceutical Co., Ltd.
Contact Information
Study Contact:
Hong Chen
+86-0518-82342973
hong.chen@hengrui.com
Interventions
  • Drug: HRS9531 — HRS9531-low dose
  • Drug: HRS9531 — HRS9531-high dose
  • Drug: Placebo — Placebo
Study Locations (1 sites)
Perking University Peoples' Hospital, Beijing, Beijing Municipality 100044 China
Eligibility Criteria
Inclusion Criteria: 1. Male or female, able and willing to provide a written informed consent 2. Diagnosed with type 2 diabetes ≥ 90 days; 3. On stable once-daily dose of basal insulin alone or in combination with metformin and/or SGLT2 inhibitor ≥ 90 days; 4. HbA1c was 7.5%\~11.0% (both inclusive); 5. Body Mass Index (BMI) ≥22 kg/m2 at screening. Exclusion Criteria: 1. A history of type 1 diabetes, specific diabetes, or secondary diabetes; 2. Have a history of severe hypoglycemia within t180 days prior to screening; 3. History of acute cardiovascular and cerebrovascular diseases within 180 days prior to screening; 4. Have a history of malignancy within 5 years; 5. Known or suspected allergy or intolerance to the investigational medicinal products or related products; 6. Participation in any clinical trial of an approved or non-approved investigational product/treatment within the last 90 days; 7. Any conditions that the Investigator judges might not be suitable to participate in the trial.
Comparison of Different Doses of Vitamin D Supplementation on Glycated Haemoglobin and Blood Glucose Parameters With Type II Diabetes Mellitus Having Vitamin d Deficiency
NCT07321223
Active, positions filled
Conditions Diabetes (DM), Vitamin D Deficiency
Phase NA
Enrollment 108
Locations 1 sites
Compensation Compensation typically provided
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

COMPARISON OF DIFFERENT DOSES OF VITAMIN D SUPPLEMENTATION ON GLYCATED HEMOGLOBIN (HbA1c) and BLOOD GLUCOSE PARAMETRS IN PATIENTS WITH TYPE 2 DIABETES MELLITUS HAVING VITAMIN D DEFICIENCY"

Design

Study type: Interventional Phases: Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: None

Interventions / Regimen

  • Dietary Supplement: Vitamin D — Vitamin D supplement capsules (50,000 IU, 200000 IU)

Primary Outcomes

  • HbA1c (90 days)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: NA
Status: Active, positions filled
Start Date: 2024-08-22
Completion: 2026-02-22
Eligibility
Age: 40 Years
Sex: ALL
Volunteers: false
Enrollment: 108 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: University of Lahore
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Dietary Supplement: Vitamin D — Vitamin D supplement capsules (50,000 IU, 200000 IU)
Study Locations (1 sites)
PAF Hospital, Islamabad, Pakistan
Eligibility Criteria
Inclusion Criteria: Patients diagnosed of T2DM with the age of 40-70 years from both genders taking only metformin with an Hb1Ac range of 7.5-9% and 25-hydroxy Vitamin D levels (25\[OH\]D) \<20ng/ml. Exclusion Criteria: Individuals Exclusion Criteria: Individuals with the following conditions will not be included as participants; * Inability or unwilling to participate or Clinical proximal myopathy * Renal, hepatic, endocrinological disorders or malignancies on basis of history * Serum calcium levels \> 10.5mg/dl * Use of insulin or any change in dosage of current hypoglycemic medications during last 3 months * Intake of vitamin D, calcium or omega 3 supplements within the past 3 months
Research on Effects of Drugs on Body Composition and Function With Imaging in Diabetes
NCT07156331
Not yet recruiting
Conditions Type 2 Diabetes
Phase Not Applicable
Enrollment 20
Locations 0 sites
Compensation Compensation varies
Data Updated 2026-07-29
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Study Details Design, interventions, and primary outcomes

About This Study

One downside of diabetes weight loss drugs like GLP-1RA and GLP-1RA/GIP, is that they can cause muscle loss, which is especially risky for older adults or those already prone to frailty and falls. There is also concern that GLP-1RA might affect bone health, possibly leading to weaker bones and increased risk of fractures. To prevent these issues, doctors need to better predict who is most at risk of muscle and/or bone loss. That way, doctors can adjust patient management-like adding targeted physical therapy, or bone-protecting medications alongside GLP-1RA or GLP-1RA/GIP medications. Medical imaging can help spot early muscle and bone changes. Advanced imaging, like PET and CT scans allow for the assessment of muscle fat content and blood flow in the bones and muscles. This could provide clearer insights into how GLP-1RA or GLP-1RA/GIP medications affect muscles and bones in ways that matter for patients (strength, mobility, falls risk, etc.). The investigators will conduct an exploratory study of 20 patients initiating on GLP-1RA or GLP-1RA/GIP by their care provider, and assess their muscle and bone health at baseline, 3, 6, and 12 months using advanced PET/CT imaging. The investigators will also assess functional measures, including grip strength, Timed Up and Go test, and gait speed. The goal is to measure and describe early changes in body composition and physical function that could signal harm. These findings will help to develop a clinical prediction tool for clinicians to use prior to starting semaglutide or tirzepatide, as well as design interventions to help promote healthy muscle and bone while on treatment.

Design

Study type: Observational Observational model: Cohort Time perspective: Prospective

Primary Outcomes

  • Change in skeletal muscle mass at 1-year (Change from baseline to 12 months)
  • Change in Timed Up-and-Go (TUG) at 1-year (Change from baseline to 12 months)
  • Change in Gait Speed at 1-year (Change from baseline to 12 months)
  • Change in Handgrip Strength at 1-year (Change from baseline to 12 months)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: OBSERVATIONAL
Phase: Not Applicable
Status: Not yet recruiting
Start Date: 2025-10-01
Completion: 2027-12-31
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 20 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Kristin Clemens
Principal Investigators:
  • Kristin Clemens, MD, MSc (PRINCIPAL_INVESTIGATOR) - St. Joseph's Health Care London
Contact Information
Study Contact:
Heather LaPier, BSc
519-646-6100
heather.lapier@sjhc.london.on.ca
Interventions
N/A
Eligibility Criteria
Inclusion Criteria: * Be at least 18 years old * Have type 2 diabetes * Have recently been started on semaglutide or tirzapatide under the care of a physician * Be able to speak and read English Exclusion Criteria: * Are pregnant or breastfeeding * Are unable to perform functional tests * Are unable to provide informed consent * Have any contraindication to PET/CT scan * Had a change in body weight over 5 kilograms within 90 days before starting a GLP-1RA or GLP-1RA/GIP * Had previous or planned (during the study period) bariatric surgery in the subsequent 12 months.
Clinical Trial Assessing Human Placental Membrane Products and Standard of Care Versus Standard of Care in Nonhealing DFUs and VLUs
NCT06674980
Recruiting
Conditions Pathologic Processes, Diabetes Mellitus,...
Phase NA
Enrollment 177
Locations 1 sites
Compensation Compensation typically provided
Data Updated 2026-07-29
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Study Details Design, interventions, and primary outcomes

About This Study

The purpose of the study is to evaluate the efficacy of multiple human placental membrane products and Standard of Care (SOC) versus SOC alone in the management of nonhealing diabetic foot ulcers (DFUs) and venous leg ulcers (VLUs) over 12 weeks using a modified platform trial design.

Design

Study type: Interventional Phases: Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: None

Interventions / Regimen

  • Other: Standard of Care - DFU — Beginning at the screening visit, participants will receive weekly treatment with standard of care (cleaning, debridement, ulcer moisture balance, and offloading) until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: AM/Single - DFU — Participants will receive weekly applications of AM/Single and Standard of Care until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: AM/Double - DFU — Participants will receive weekly applications of AM/Double and Standard of Care until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: Standard of Care - VLU — Beginning at the screening visit, participants will receive weekly treatment with standard of care (cleaning, debridement, ulcer moisture balance, and compression) until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: AM/Single - VLU — Participants will receive weekly applications of AM/Single and Standard of Care until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: AM/Double - VLU — Participants will receive weekly applications of AM/Double and Standard of Care until ulcer closure, or a maximum of 12 weeks, whichever occurs first.

Primary Outcomes

  • Determine the percentage of subjects achieving complete closure of target ulcer over 12 weeks. (1-12 weeks)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: NA
Status: Recruiting
Start Date: 2024-12-20
Completion: 2027-01-22
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 177 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: C5 Biomedical
Collaborators: SerenaGroup, Inc.
Principal Investigators:
  • Thomas Serena, MD (PRINCIPAL_INVESTIGATOR) - SerenaGroup, Inc.
Contact Information
Study Contact:
Bennett Rogers
888-960-1343
Brogers@serenagroups.com
Connie Chung, PhD
734-730-3058
Connie@c5biomedical.com
Interventions
  • Other: Standard of Care - DFU — Beginning at the screening visit, participants will receive weekly treatment with standard of care (cleaning, debridement, ulcer moisture balance, and offloading) until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: AM/Single - DFU — Participants will receive weekly applications of AM/Single and Standard of Care until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: AM/Double - DFU — Participants will receive weekly applications of AM/Double and Standard of Care until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: Standard of Care - VLU — Beginning at the screening visit, participants will receive weekly treatment with standard of care (cleaning, debridement, ulcer moisture balance, and compression) until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
  • Other: AM/Single - VLU — Participants will receive weekly applications of AM/Single and Standard of Care until ulcer closure, or a maximum of 12 weeks, whichever occurs first.
Study Locations (1 sites)
Poirot Podiatry, Metairie, Louisiana 70001 United States
Eligibility Criteria
Inclusion Criteria for DFU: 1. At least 18 years of age or older. 2. Must have diagnosis of type 1 or 2 Diabetes mellitus. 3. At enrollment, subject must have a target ulcer with a minimum surface area of 0.7 cm2 and a maximum surface area of 20.0 cm2 measured post debridement with the imaging device. 4. Must have a target ulcer that has been present for a minimum of 4 weeks and maximum of 52 weeks of standard of care, prior to screening visit. 5. Target ulcer located on the foot with at least 50% of the ulcer below the malleolus. 6. Target ulcer that is Wagner 1 or 2 grade, extending at least through the dermis or subcutaneous tissue and may involve the muscle provided it is below the medial aspect of the malleolus. The ulcer may not include exposed tendon or bone. 7. Subject's affected limb must have adequate perfusion confirmed by vascular assessment. Any of the following methods performed within 3 months of the first screening visit are acceptable: 1. ABI between 0.7 and \<= 1.3 2. TBI \>= 0.6 3. TCOM \>= 40 mmHg 4. PVR: biphasic 8. If subject has two or more ulcers, they must be separated by 2 cm. The largest ulcer satisfying the inclusion and exclusion criteria will be designated as the target ulcer. 9. Target ulcer must be located on the plantar aspect of the foot and must be offloaded for at least 14 days prior to enrollment. 10. Subject must consent to using the prescribed offloading method for the duration of the study. 11. Subject must agree to attend weekly study visits. 12. Subject must be willing and able to participate in the consent process. Exclusion Criteria for DFU: 1. Subject is known to have a life expectancy of \< 6 months. 2. Subject's target ulcer is not secondary to diabetes. 3. Target ulcer is infected or there is cellulitis in the surrounding skin. 4. Target ulcer exposes tendon or bone. 5. Evidence of osteomyelitis complicating the target ulcer. 6. Infection in the target ulcer or in a remote location that requires systemic antibiotic therapy. 7. The subject is receiving immunosuppressants (including systemic corticosteroids at doses greater than 10 mg of prednisone per day or equivalent) or cytotoxic chemotherapy or is taking medications that the PI believes will interfere with wound healing (e.g., biologics). 8. Subject is taking hydroxyurea. 9. Subject has applied topical steroids to the ulcer surface within one month of initial screening. 10. Subject has a previous partial amputation on the affected foot that results in a deformity that impedes proper offloading of the target ulcer. 11. Subject has a glycated hemoglobin (HbA1c) greater than or equal to 12% within 3 months of the initial screening visit. 12. The surface area of the subject's target ulcer has reduced in size by more than 20% in the 2 weeks prior to the initial screening visit ("historical" run-in period). Imaging Device is not required for measurements taken during the historical run-in period (e.g., calculating surface area using length X width is acceptable). 13. The surface area measurement of the subject's target ulcer decreases by 20% or more during the active 2-week screening phase. 14. Subject has acute Charcot foot, or an inactive Charcot foot, which impedes proper offloading of the target ulcer. 15. Subject is a woman who is pregnant or considering becoming pregnant in the next 6 months. 16. Subject has end stage renal disease requiring dialysis. 17. Subject has participated in a clinical trial involving treatment with an investigational product within the previous 30 days. 18. The subject, in opinion of the Investigator, has a medical or psychological condition that may interfere with study assessments. 19. Subject was treated with hyperbaric oxygen therapy or a Cellular, Acellular, Matrix-like Product (CAMP) in the 30 days prior to screening. 20. Subject has a malnutrition indicator score \<17 as measured on the Mini Nutritional Assessment. Inclusion Criteria for VLU: Potential subjects are required to meet all the following criteria for enrollment in the study. 1. Subjects must be at least 18 years of age or older. 2. At randomization subjects must have a target ulcer with a minimum surface area of 0.7 cm2 and a maximum surface area of 20 cm2 measured post-debridement. 3. The target ulcer must have been present for a minimum of 4 weeks and a maximum of 52 weeks of standard of care prior to the initial screening visit. 4. No visible signs of healing objectively, less than 40% reduction in wound size in the last 4 weeks. 5. The affected limb must have adequate perfusion confirmed by vascular assessment. Any of the following methods performed within 3 months of the first screening visit are acceptable: 1. ABI between 0.7 and ≤ 1.3; 2. TBI ≥ 0.6; 3. TCOM ≥ 40 mmHg; 4. PVR: biphasic. 6. If the potential subject has two or more ulcers, they must be separated by at least 2 cm post-debridement. The largest ulcer satisfying the inclusion and exclusion criteria will be designated as the target ulcer. 7. The potential subject must agree to attend the weekly study visits required by the protocol. 8. The potential subject must be willing and able to participate in the informed consent process. Exclusion Criteria for VLU: 1. The potential subject is known to have a life expectancy of \< 6 months. 2. The target ulcer is infected, requires systemic antibiotic therapy, or there is cellulitis in the surrounding skin. 3. The target ulcer exposes tendon or bone. 4. There is evidence of osteomyelitis complicating the target ulcer. 5. The potential subject is receiving immunosuppressants (including systemic corticosteroids at doses greater than 10 mg of prednisone per day or equivalent) or cytotoxic chemotherapy or is taking medications that the PI believes will interfere with wound healing (e.g., biologics). 6. The potential subject has applied topical steroids to the ulcer surface within one month of initial screening. 7. The potential subject has glycated hemoglobin (HbA1c) greater than or equal to 12% within 3 months of the initial screening visit. 8. The surface area of the target ulcer has reduced in size by more than 20% in the 2 weeks prior to the initial screening visit ("historical" run-in period). Imaging Device is not required for measurements taken during the historical run-in period (e.g., calculating surface area using length X width is acceptable). 9. The surface area measurement of the target ulcer decreases by 20% or more during the active 2-week screening phase: the 2 weeks from the initial screening visit (SV-1) to the TV-1 visit during which time the potential subject received SOC. 10. Women who are pregnant or considering becoming pregnant within the next 6 months. 11. The potential subject has end stage renal disease requiring dialysis. 12. Participation in a clinical trial involving treatment with an investigational product within the previous 30 days. 13. A potential subject who, in the opinion of the investigator, has a medical or psychological condition that may interfere with study assessments. 14. The potential subject was treated with hyperbaric oxygen therapy (HBOT) or a Cellular, Acellular, Matrix-like Product (CAMP) in the 30 days prior to the initial screening visit. 15. The subject has a malnutrition indicator score \<17 as measured on the Mini Nutritional Assessment. 16. A subject has a wound with active or latent infection is excluded. 17. A subject with a disorder that would create unacceptable risk of post-operative complications is excluded.
Genetics of Response to Canagliflozin
NCT02891954
Active, positions filled
Conditions Diabetes Mellitus, Type 2
Phase PHASE1
Enrollment 700
Locations 0 sites
Compensation Phase 1: Typically $1,000-$5,000
Data Updated 2026-07-29
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Study Details Design, interventions, and primary outcomes

About This Study

Five daily doses of canagliflozin (300 mg) will be administered to healthy volunteers. Pharmacodynamic responses to canagliflozin will be assessed both at 2 days and 6 days after administration of the first dose of canagliflozin. A genome-wide association study (GWAS) will be conducted to search for genetic variants that are associated with each of the pharmacodynamic responses to canagliflozin.

Design

Study type: Interventional Phases: Phase1 Allocation: Intervention model: Single Group Primary purpose: Basic Science Masking/blinding: None

Interventions / Regimen

  • Drug: Canagliflozin — Healthy volunteers will receive canagliflozin (300 mg per day) in the morning for five days.

Primary Outcomes

  • Urinary glucose excretion (during the time interval 24-48 hours after first administration of canagliflozin) (24-48 hours)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE1
Status: Active, positions filled
Start Date: 2016-09
Completion: 2026-12-25
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: true
Enrollment: 700 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: University of Maryland, Baltimore
Collaborators: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Principal Investigators:
  • Simeon I Taylor, MD, PhD (PRINCIPAL_INVESTIGATOR) - Unversity of Maryland School of Medicine
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Drug: Canagliflozin — Healthy volunteers will receive canagliflozin (300 mg per day) in the morning for five days.
Eligibility Criteria
Inclusion Criteria: * Of Amish descent * Age 18 or older * BMI: 18-40 kg/m2 Exclusion Criteria: * Known allergy to canagliflozin * History of diabetes, random glucose greater than 200 mg/dL, or HbA1c greater than or equal to 6.5% * Currently taking diuretics, antihypertensive medication uric acid lowering medications, or other medication that the investigator judges will make interpretation of the results difficult * Significant debilitating chronic cardiac, hepatic, pulmonary, or renal disease or other diseases that the investigator judges will make interpretation of the results difficult or increase the risk of participation * Seizure disorder * Unwilling to go off of vitamin supplements and over the counter medication (except for acetaminophen) for at least two weeks prior to the first home visit and agree to avoid these medications for the duration of the study. * Positive urine human chorionic gonadotropin test or known pregnancy within 3 months of the start of the study * Estimated glomerular filtration rate less than 60 mL/min * Currently breast feeding or breast feeding within 3 month of the start of the study * Liver function tests greater than 2 times the upper limit of normal * Hematocrit less than 35% * Abnormal thyroid hormone stimulating hormone
A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly Incretin
NCT07392190
Recruiting
Conditions Overweight, Obesity
Phase PHASE3
Enrollment 900
Locations 173 sites
Compensation Phase 3: Typically $200-$1,000
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo in participants with persistent obesity or overweight, with or without type 2 diabetes, and on stable incretin background therapy. Participation in the study will last about 80 weeks.

Design

Study type: Interventional Phases: Phase3 Allocation: Randomized Intervention model: Parallel Primary purpose: Treatment Masking/blinding: Double

Interventions / Regimen

  • Drug: Eloralintide — Administered SC
  • Drug: Placebo — Administered SC

Primary Outcomes

  • Percent Change from Baseline in Body Weight (Baseline, Week 64)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: PHASE3
Status: Recruiting
Start Date: 2026-02-10
Completion: 2028-07
Eligibility
Age: 18 Years
Sex: ALL
Volunteers: false
Enrollment: 900 (ESTIMATED)
Sponsor & Investigators
Lead Sponsor: Eli Lilly and Company
Principal Investigators:
  • Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST) (STUDY_DIRECTOR) - Eli Lilly and Company
Contact Information
Study Contact:
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
317-615-4559
LillyTrials@Lilly.com
Physicians interested in becoming principal investigators please contact
clinical_inquiry_hub@lilly.com
Interventions
  • Drug: Eloralintide — Administered SC
  • Drug: Placebo — Administered SC
Study Locations (173 sites)
Birmingham Clinical Research, Birmingham, Alabama 35209 United States
RIO Clinical Trials - Phoenix, Phoenix, Arizona 85016 United States
Headlands Research - Scottsdale, Scottsdale, Arizona 85260 United States
Novak Clinical Research - Tucson - North La Cholla Boulevard, Tucson, Arizona 85741 United States
Irvine Clinical Research, Irvine, California 92614 United States
Scripps Whittier Diabetes Institute, La Jolla, California 92037 United States
EndoTrials Center for Clinical Research, La Mesa, California 91942 United States
Peninsula Research Associates, Rolling Hills Estates, California 90274 United States
Care Access - Sacramento, Sacramento, California 95831 United States
Artemis Institute for Clinical Research, San Diego, California 92123 United States
Eligibility Criteria
Inclusion Criteria: * Are on stable incretin therapy at screening * With persistent obesity or overweight defined as: * ≥30 kg/m2 OR * ≥27 kg/m2 with at least one existing obesity related complication at screening: * hypertension * dyslipidemia * obstructive sleep apnea * cardiovascular disease (for example, ischemic cardiovascular disease, New York Heart Association Functional Class I-III heart failure), or * type 2 diabetes * Have a stable body weight (\<5% body weight change) at screening Exclusion Criteria: * Have a prior or planned surgical treatment for obesity (liposuction, cryolipolysis, or abdominoplasty allowed if performed \>1 year before screening) * Have a prior or planned endoscopic procedure and/or device-based therapy for obesity (prior device-based therapy acceptable if device removal was more than 6 months prior to screening) * Have type 1 diabetes * Have taken any of the following antihyperglycemic medications within 90 days before screening: * dipeptidyl peptidase-4 (DPP-4) inhibitors * amylin analogs * insulin * Have had within 90 days prior to screening: * heart attack * stroke * coronary artery revascularization * unstable angina, or * hospitalization due to congestive heart failure * Have a history or diagnosis of New York Heart Association Functional Classification Class IV congestive heart failure
Safety and Efficacy Assessment of Unani Formulation 'Dolabi' in Management of Diabetes Mellitus Type II
NCT06841497
Active, positions filled
Conditions Diabetes Mellitus, Type 2 DM
Phase NA
Enrollment 100
Locations 1 sites
Compensation Compensation typically provided
Data Updated 2026-07-29
Click to view full details
Study Details Design, interventions, and primary outcomes

About This Study

Diabetes is a chronic health condition that affects millions of people worldwide. In recent years, Pakistan has witnessed a significant increase in the prevalence of diabetes, making it a major public health concern. To address this growing problem, conducting clinical trials on diabetes in Pakistan is of utmost importance. Clinical trials play a crucial role in advancing medical knowledge, improving patient care, and finding effective treatments for diabetes. This research aims to assess the safety and effectiveness of the Unani formulation Dolabi in treating type II diabetes mellitus. The study consists of two phases: a pre-clinical phase, which involves acute and subacute oral toxicity testing on animal models, and a clinical phase, which includes a single-blind, single-arm, multicenter, phase II clinical trial conducted at Shifa ul Mulk Memorial Hospital-Hamdard University and Haidery Herbal Care-North Nazimabad to evaluate its clinical efficacy. Diabetes management plays a vital role in effectively controlling the disease and minimizing its complications. Lifestyle management plays significant role in managing blood glucose levels in all age and gender segments. Medications are prescribed to regulate blood glucose levels when lifestyle changes alone are insufficient. Regular monitoring of blood sugar levels, along with other important parameters like blood pressure and cholesterol, helps individuals with diabetes to track their progress and make necessary adjustments to their treatment plans. Dolabi is a time tested formulation of HLWP and it is being used clinically for more than 05 years at Hamdard Matabs all around Pakistan and clinically found satisfactory. The current study is designed in accordance with ICH GCP E6 protocols as approved by WHO and DRAP. It will enable us to present this safer and locally produced combination for the large community suffering with this condition in improving their lives.

Design

Study type: Interventional Phases: Allocation: Intervention model: Single Group Primary purpose: Treatment Masking/blinding: None

Interventions / Regimen

  • Other: Dolabi — herbal remedy for DM II

Primary Outcomes

  • Blood Sugars (12 weeks)
  • HbA1C (Glycosylated Hemoglobin) (12 weeks)
Interested in this trial?
Contact the study team directly or view the official listing
Study Information
Type: INTERVENTIONAL
Phase: NA
Status: Active, positions filled
Start Date: 2024-07-04
Completion: 2025-10-03
Eligibility
Age: 30 Years
Sex: ALL
Volunteers: false
Enrollment: 100 (ACTUAL)
Sponsor & Investigators
Lead Sponsor: Hamdard University
Contact Information
No direct contact listed - use the ClinicalTrials.gov link below to reach the study team
Interventions
  • Other: Dolabi — herbal remedy for DM II
Study Locations (1 sites)
Shifa Ul Mulk Memorial Hospital-Hamdard University, Karachi, Sindh 74600 Pakistan
Eligibility Criteria
Inclusion Criteria: * Subjects having Type II Diabetes Mellitus. * Subjects having raised FBS above 120 mg/dl and HbA1C level 6.7 or above. * Subjects over 30 years of age. * Subjects agree to use study medicine throughout the study. Exclusion Criteria: * Subjects suffering from chronic liver diseases and kidney failure. * Subjects currently taking any hypoglycemic agent(s). * Subjects suffering from any type of cancer and any other comorbid condition. * Subjects having history of adverse drug reaction. * Pregnant and Lactating mother.