Recruiting
PARTial BREast RECONstruction With Chest Wall Perforator Flap
The goal of this observational study is to ascertain the outcomes following partial breast reconstruction using chest wall perforator flaps after breast conservation surgery.
ClinicalTrials.gov IDNCT06728527
PhaseNot Applicable
Enrollment1001
SponsorCambridge University Hospitals NHS Foundation Trust
Age18 Years
SexFEMALE
Conditions studied
Breast Cancer Early Stage Breast Cancer (Stage 1-3), Breast Carcinoma, Breast Neoplasms, Breast Surgery, Breast Reconstruction Surgery
About this study
The goal of this observational study is to ascertain the outcomes following partial breast reconstruction using chest wall perforator flaps after breast conservation surgery.
Primary outcomes
- Surgical Complications (Within 30 days of surgery)
Eligibility information
Inclusion Criteria:
* Patients undergoing partial breast reconstruction using CWPF for primary breast cancer
* Delayed correction of breast deformity following previous BCS
* Each surgeon is to have performed a minimum of 10 CWPFs
* Each centre anticipates completing a minimum of 10/year
Exclusion Criteria:
* Patients undergoing volume displacement BCS
* Patients undergoing mastectomy +/- immediate breast reconstruction
Study locations
- Cambridge University Hospitals NHS Trust, Cambridge, Cambridgeshire CB2 0QQ United Kingdom
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.