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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