Condition: Gender Dysphoria · Mastectomy · Hypertrophic Scar · Sponsor: University of California, San Francisco
The goal of this randomized, prospective, interventional clinical trial is to evaluate the use of Brijjit® in reducing the incidence of hypertrophic scarring in individuals undergoing gender-affirming bilateral double incision mastectomies at a single-institution, single-surgeon site (Esther A. Kim, MD). Patients will serve as a self-control (one side of the chest receives intervention, the other serves as a control). Primary endpoints include scar appearance and quality. Secondary endpoints include patient perception of the scar using the Patient and Observer Scar Assessment Scale (POSAS). Participants will be taught how to apply Brijjit® at home if any units fall off before 6 weeks postop.
This description comes directly from the study's public registry record.
Nathan S Ramrakhiani, BS · 6507760834 · nathan.ramrakhiani@ucsf.edu
Lindsay A Tao, BS · 7603300915 · lindsay.tao@ucsf.edu
Always discuss trial participation with your own doctor first.
| UCSF Department of Plastic & Reconstructive Surgery | San Francisco, California, United States | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT07147166