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PARTial BREast RECONstruction With Chest Wall Perforator Flap (PartBreCon)

NHS Foundation Trust logo

NHS Foundation Trust

Status

Enrolling

Conditions

Breast Reconstruction Surgery
Breast Cancer Early Stage Breast Cancer (Stage 1-3)
Breast Surgery
Breast Neoplasms
Breast Carcinoma

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this observational study is to ascertain the outcomes following partial breast reconstruction using chest wall perforator flaps after breast conservation surgery.

Full description

The Main Outcomes and Measures are:

A) Patient Demographics and Tumour characteristics

  1. Patient demographics: age, body mass index (BMI), comorbidities
  2. Preoperative tumour characteristics and location influencing surgical planning

B) Treatment characteristics

  1. Surgical: operative data, including flap types and distribution
  2. Oncological: systemic therapies (adjuvant and neoadjuvant), radiotherapy

Enrollment

1,001 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Amit Agrawal, DM, FRCS

Data sourced from clinicaltrials.gov

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