Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03754218Phase 1Completed
Phase 1, open-label trial of amnion membrane powder in burn injury and skin wound (2 arms), sponsored by Wake Forest University Health Sciences. Primary endpoint: Incidence of Donor Site Wound Closure at 4 weeks. Started Dec 2019; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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