RecruitingNCT07546331

Novel Body Composition Measurements in Association With Outcomes of Breast Reconstruction Reconstruction

Investigation Into the Utility of Novel Body Composition Measurements in Association With Outcomes of Breast Reconstruction

Sponsor

University of California, San Francisco

Enrollment

40 participants

Start Date

Feb 18, 2026

Study Type

OBSERVATIONAL

Conditions

This study compares measurements of body composition to outcomes of breast reconstruction.

Min Age: 18 Years

Patients must have histologically confirmed breast malignancy or increased risk of developing a breast malignancy.
Age ≥ 18 years.
Scheduled to undergo mastectomy with immediate breast reconstruction using a permanent implant, tissue expander, or autologous tissue (e.g. Deep Inferior Epigastric Perforator (DIEP) flap, muscle-sparing Transverse Rectus Abdominis Myocutaneous (msTRAM) flap, Profunda Artery Perforator (PAP) flap).
Ability to understand a written informed consent document, and the willingness to sign it.

Any significant medical condition or laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study.
Pregnant or breastfeeding.
Patients assigned male at birth.
Non-cisgender women.
Patients with implanted electronic medical devices (e.g. pacemaker, defibrillator).
Patients with prosthetic limbs.

Interested in this trial?

Get notified about updates and connect with the research team.

PROCEDUREMeasurement of Body Composition

Body composition measurements collected pre and post operatively using a bioelectrical impedance analyzer.

OTHERChart Review

Clinical and surgical data will be collected from the participants medical records.

University of California

San Francisco, California, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

NCT07546331