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Amniotic Membrane in Decompressive Craniectomy to Reduce Scarring

Scarring Clinical Trial

Official title:
A Multicenter Prospective Randomized Clinical Trial Using Dehydrated Human Amnion/Chorion Membrane dHACM in Decompressive Craniectomy Patients to Reduce Postoperative Scarring

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of dHACM in reducing scar tissue formation in craniectomy patients as well as facilitating reoperation and repair. Specifically this study compares craniectomy without dHACM application to craniectomy with placement of dHACM between the galea and dura over dural suture line and/or exposed parenchyma.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02033824
Study type Interventional
Source MiMedx Group, Inc.
Contact
Status Completed
Phase N/A
Start date April 2014
Completion date June 2018
View Details
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