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Amniotic Membrane in Total Knee Replacements to Reduce Scarring

Scarring Clinical Trial

Official title:
A Prospective Randomized Clinical Trial Using Dehydrated Human Amnion/Chorion Membrane (dHACM) in Total Knee Replacement Patients to Reduce Post-operative Scarring.

Clinical Trial Summary

The overall objective of this study is to evaluate the effectiveness of dHACM in reducing scar tissue formation in total knee replacement patients.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02088567
Study type Interventional
Source MiMedx Group, Inc.
Contact
Status Completed
Phase N/A
Start date January 2014
Completion date October 2014
View Details
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