About this trial

The overall objective of this proposal is to conduct a randomized-controlled study to determine whether treatment with dehydrated human amnion/chorion membrane (dHACMs) allografts can improve NAC viability in patients undergoing nipple sparing mastectomy (NSM). dHACM allografts are commercially available tissue membranes with biocompatible extracellular matrix and growth factors that have been shown to improve wound healing in patients with chronic and lower extremity wounds. To date, no study has evaluated the impact of dHACMs on NAC preservation following NSM. Investigators hypothesize that subareolar surgical implantation of dHACM allografts at time of NSM will reduce NAC necrosis and improve viability.

Eligibility criteria

Qualifiers

Biologically female with documented diagnosis of gender dysphoria, desire to undergo gender affirming surgery (female-to-male) NSM, and age 15 years of age or older.

Biological female, age 18 to 75 years old, who desire to undergo bilateral prophylactic NSM for nonmalignant breast conditions or to reduce the risk of breast cancer.

Disqualifiers

Current steroid use

Known connective tissue disorder

Known neuropathy

Known history of breast cancer

Trial design

Treatments tested in this trial

  • AmnioFix dehydrated Human Amnion/Chorion Membrane Allograft
  • Control Device

Treatment groups

30 Participants
are divided into 2 treatment groups

Locations

1
Division of Plastic & Reconstructive Surgery94304, Palo AltoCalifornia, United States

Sponsors and collaborators

Stanford University

Lead sponsor