Oasis Donor Site Wounds Post-Market Study

Status Recruiting

Clinical Trial Summary

The purpose of this study is to demonstrate the safety and performance of Oasis extracellular matrix (ECM) when used as a treatment for donor site wounds in the United Kingdom. Oasis ECM is commercially available for the treatment of partial and full-thickness skin wounds, including chronic wounds, wounds from trauma, and wounds that occur during surgery, such as donor site wounds. The ability of the Oasis ECM to promote the healing of donor site wounds will be evaluated in this study. About 40 patients (20 in each arm) over 16 years old will be involved in this study at one center in the United Kingdom.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04079348
Study type	Interventional
Source	Cook Biotech Incorporated
Contact	Jason Hodde, MS
Phone	765-497-3355
Email	jhodde@rtix.com
Status	Recruiting
Phase	N/A
Start date	November 1, 2020
Completion date	December 2025

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