๐๏ธ Verified NIH Record โข Updated 2026-04-29
Acellular Dermal Matrix Investigation in Breast Reconstruction (NCT06456554)
๐ข Recruiting Observational / Diagnostic โ๏ธ Medical Device Protocol Sponsor: RTI Surgical
๐ฉบ Plain-English Summary (8th-Grade Level)
Prospective, multi-center, dual-arm non-randomized clinical study in females undergoing a two-stage breast reconstruction using a pre-pectoral technique.
Who can join: Review the eligibility criteria below.
Location: University of Arkansas โ Little Rock, Arkansas
Age range: 22 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (13 Sites)
- University of Arkansas โ Little Rock, Arkansas
- City of Hope National Medical Center โ Duarte, California
- University of Colorado โ Aurora, Colorado
- University of Kansas โ Lawrence, Kansas
- Washington University โ St Louis, Missouri
- Mercy Hospital โ St Louis, Missouri
- NYU Langone Health โ New York, New York
- New York Presbyterian Hospital/Columbia University Irving Medical Center โ New York, New York
- Cleveland Clinic โ Cleveland, Ohio
- Mercy Hospital โ Oklahoma City, Oklahoma
- Mercy โ Oklahoma City, Oklahoma
- University of Pennsylvania โ Philadelphia, Pennsylvania
- MD Anderson โ Houston, Texas
๐ Contact the Study Coordinator
Phone: (202) 552-6013
Email: avillagomez@mcra.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ 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.
More studies in Breast Reconstruction
- Pre- Versus Sub-pectoral Implant-based Breast Reconstruction After Skin-sparing Mastectomy or Nipple-sparing Mastectomy OPBC-02PREPEC โ Boston, Massachusetts
- A Study of the Safety and Effectiveness of the Mentor Larger Size MemoryGel Ultra High Profile Breast Implants in Subjects Who Are Undergoing Primary Breast Reconstruction or Revision Reconstruction โ Montgomery, Alabama
- Evaluation of the Safety and Effectiveness of ARTIA Reconstructive Tissue Matrix Breast Reconstruction (ADORA) in Adult Participants โ Los Angeles, California
- Access My Breast Cancer Care App โ Vancouver, British Columbia
- Impact of Pectoral Versus Paravertebral Blocks on Pain and Physical Well-Being in Implant-Based Breast Reconstruction โ Boston, Massachusetts
Explore by condition: All Breast Reconstruction clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.