Recruiting
Effects of Change in Blood Pressure on Retinal Capillary Rarefaction in Patients With Arterial Hypertension
To evaluate whether in patients with initially poorly-controlled arterial hypertension, structural and functional differences in the retina and choroid remain after achieving a well-controlled blood pressure.
ClinicalTrials.gov IDNCT06098300
PhaseNot Applicable
Enrollment30
SponsorMedical University of Vienna
Age18 Years
SexALL
Conditions studied
Arterial Hypertension, Blood Pressure, High
About this study
To evaluate whether in patients with initially poorly-controlled arterial hypertension, structural and functional differences in the retina and choroid remain after achieving a well-controlled blood pressure.
Primary outcomes
- Change in retinal vessel density after achieving blood pressure treatment target (OCT-A). (12 weeks)
Eligibility information
Inclusion Criteria:
* Men and Women aged ≥ 18 years
* Signed informed consent
* Apart from hypertensive retinopathy, normal ophthalmic findings
* Non-Smokers
* Patients with initially diagnosed or pre-existing mild to moderate primary arterial hypertension (systolic office blood pressure ≥ 140 mmHg and/or diastolic office blood pressure ≥ 90 mmHg)
* Planned initiation of antihypertensive medication or planned adaption of antihypertensive medication by the Department of Cardiology
* Subject agrees to perform regular blood pressure self-measurements and to document blood pressure values in a diary
Exclusion Criteria:
* Participation in a clinical trial in the three weeks preceding the study
* Blood donation in the three weeks preceding the study
* Symptoms of a clinically relevant illness in the three weeks preceding the study
* History of family history of epilepsy
* Secondary hypertension (e.g.: hyperaldosteronism, pheochromocytoma, renal artery stenosis, renal parenchymal diseases, Cushing-syndrome, Coarctatio aortae)
* History of hypertensive encephalopathy or intracerebral bleeding
* Diabetes mellitus Type 1 or Type 2
* Pregnant or breast-feeding women
* Women of childbearing potential (neither menopausal, nor hysterectomized, nor sterilized) not using effective contraception
Study locations
- Medical University of Vienna, Vienna, 1090 Austria
Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.