dHACM Mesh In the Treatment of Diabetic Foot Ulcers

Status Completed

Clinical Trial Summary

A single-centered, non-randomized study with approximately 20 subjects that will be seen for up to 12 weeks, each receiving the EpiFix mesh plus standard of care. Safety and effectiveness will be monitored throughout the study.

Clinical Trial Description

Approximately 20 subjects will be enrolled in this study. Subjects will be seen for up to12 weeks unless 100% epithelialization of the index wound and two subsequent healing confirmation visits have been achieved prior to week 12. Each subject will receive a weekly application of the EpiFix Mesh plus standard of care until 100% epithelialization is achieved. The subjects will be evaluated for efficacy and safety during the course of the trial. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02589210
Study type	Interventional
Source	MiMedx Group, Inc.
Contact
Status	Completed
Phase	N/A
Start date	May 2015
Completion date	March 2016

View Details

See also
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