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Facial Vascularized Composite Allotransplantation: A Study Evaluating Safety, Functional Outcomes, and Patient-Reported Psychosocial Outcomes

StatusNot Yet Recruiting
PhaseNot applicable
Started2027-10
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487 trials monitored
See 35 trials at risk
The primary objective of this study is to evaluate the 5-year (60-month) allograft survival rate of facial vascularized composite allotransplantation performed under the standardized CONSORT clinical protocol.
Trial Details
NCT Number NCT07810764
Lead Sponsor Yale University
Collaborators: Wake Forest University Health Sciences
Conditions Facial Vascularized Composite Allotransplantation, Functional Recovery
Enrollment 5 participants
Start Date 2027-10
Primary Completion 2037-10 (estimated)
Study Completion 2037-10 (estimated)
Updated on ClinicalTrials.gov 2026-09-09