DHACM vs Other Commercially Available Treatments

Status Completed

Clinical Trial Summary

The purpose of this study is to determine whether dehydrated human amnion/chorion membrane (dHACM) is more effective than another commercially available product or conservative measures alone when used to treat diabetic foot ulcers (DFUs).

Clinical Trial Description

This is a prospective, stratified, randomized, controlled, comparative, parallel group, multi-center clinical trial comparing the proportion of ulcers completely healed by use of dehydrated human amnion/chorion membrane (dHACM) placed weekly versus placement of bioengineered skin substitute (BSS) placed weekly, versus standard of care in diabetic patients with a diabetic foot ulcer who have adequate arterial perfusion as defined in section, 2.0 (Patient Eligibility), for wound healing to the affected limb. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01921491
Study type	Interventional
Source	MiMedx Group, Inc.
Contact
Status	Completed
Phase	N/A
Start date	August 2013
Completion date	September 2015

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See also
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