Condition: Breast Cancer · Breast Implant; Complications, Infection or Inflammation · Sponsor: University of California, Los Angeles
Surgical mesh products, particularly acellular dermal matrices (ADM), are now used by the majority of plastic surgeons to assist with the nearly 100,000 prosthetic breast reconstruction procedures in the United States, despite never being approved by Food and Drug Administration (FDA) for this indication. As surgeons transition to placing breast implants above the chest muscle (pre-pectoral), there has been an increasing reliance on these often expensive mesh products without robust evidence to understand their risks and benefits. Our pilot study is a randomized multi-center trial to evaluate surgical mesh assistance in pre-pectoral tissue expander to breast implant reconstruction to address vital questions for women's public health.
This description comes directly from the study's public registry record.
Michael Delong, MD · (310) 825-5510 · mdelong@mednet.ucla.edu
Jaco Festekjian, MD · (310) 825-5510
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| University of California Los Angeles | Los Angeles, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05190978