Amniotic Membrane in Total Knee Replacements to Reduce Scarring

Completed · Not applicable

Conditions studied: Scarring

In brief

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

Key facts

Study ID
NCT02088567
Run by
MiMedx Group, Inc.
People needed
52
Starts
2014-01-01
Expected to finish
2014-10-01
Last updated by the study team
2015-09-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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