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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


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

See also
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