PEP on a Skin Graft Donor Site Wound

Status Active, not recruiting

Clinical Trial Summary

The purpose of this study is to determine the safety of a biological therapeutic PEP in participants who have skin graft donor site wounds.

Clinical Trial Description

This is an open label phase 1b study of PEP (a leukocyte depleted blood preparation derived from human U.S. sourced pooled apheresed platelets) in patients with at least two donor split-thickness skin graft wounds. One donor site will be treated with the standard post-operative dressing, while the other site will be treated with PEP or PEP+TISSEEL and covered with a standard dressing. TISSEEL is a commercially available fibrin sealant. ;

Study Design

Related Conditions & MeSH terms

Skin Graft

Clinical Trial Details

NCT number	NCT04664738
Study type	Interventional
Source	Rion Inc.
Contact
Status	Active, not recruiting
Phase	Phase 1
Start date	March 16, 2021
Completion date	February 2, 2024

View Details

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