๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-02-13

A Study of the Use of Acellular Dermal Matrix for Breast Reconstruction (NCT05316324)

A Randomized Controlled Trial of Prepectoral Breast Reconstruction With and Without Acellular Dermal Matrix

๐Ÿ”ต Active, Not Recruiting Phase3 ๐Ÿฉบ Clinical Procedure Protocol Sponsor: Memorial Sloan Kettering Cancer Center

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The researchers are doing this study to look at the number of complications that occur immediately after prepectoral breast reconstruction when Acellular Dermal Matrix (ADM) is used compared to when ADM is not used. These complications include infections, the need for Tissue Expander (TE) or implant removal, and other conditions that lead to additional surgery.

Who can join: Review the eligibility criteria below.

Location: Memorial Sloan Kettering Cancer Center (All Protocol Activities) โ€” New York, New York

Age range: 21 Years to 75 Years

๐Ÿงช Interventions in This Study

  • Prepectoral Breast Reconstruction with Acellular Dermal Matrix (ADM) (PROCEDURE)
  • Prepectoral Breast Reconstruction without Acellular Dermal Matrix (ADM) (PROCEDURE)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (2 Sites)

  • Memorial Sloan Kettering Cancer Center (All Protocol Activities) โ€” New York, New York
  • Memorial Sloan Kettering Nassau (Limited Protocol Activities) โ€” Rockville Centre, New York

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 525-2225

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Breast Cancer clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—