Clinical trial
A Study to Evaluate the Safety and Effectiveness of AlloMend® Acellular Dermal Matrix Used in Post Mastectomy Pre-Pectoral Breast Reconstruction and Followed for Up To 12-Months Post-Operatively
NCT06853964 is registered in ClinicalTrials.gov with AlloSource as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Study to Evaluate the Safety and Effectiveness of AlloMend® Acellular Dermal Matrix Used in Post Mastectomy Pre-Pectoral Breast Reconstruction and Followed for Up To 12-Months Post-Operatively
- Lead sponsor
- AlloSource
- Phase
- Observational
- Overall status
- Active, not recruiting
- Start date
- January 27, 2025
- Completion date
- May 31, 2026
- Enrollment
- 100 (estimated)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
pre-pectoral breast reconstruction following mastectomy