Clinical Trials Directory

Trials / Completed

CompletedNCT01357187

An Evaluation of the Effect of the AmnioFix Amniotic Membrane Allograft in Patients Undergoing Posterior Instrumentation Removal

An Evaluation of the Effect of the AmnioFix™ Amniotic Membrane Allograft on Scar Tissue and Adhesions in Patients Undergoing Posterior Instrumentation Removal

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
5 (actual)
Sponsor
MiMedx Group, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate the clinical effectiveness of AmnioFix™ in the reduction of the tenacity and frequency of soft tissue adhesions during the removal of segmental posterior lumbar instrumentation.

Conditions

Interventions

TypeNameDescription
OTHERScheduled removal of posterior instrumentation with AmnioFix
OTHERScheduled removal of posterior instrumentation without AmnioFix

Timeline

Start date
2011-09-01
Primary completion
2014-05-01
Completion
2014-05-01
First posted
2011-05-20
Last updated
2015-03-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01357187. Inclusion in this directory is not an endorsement.

An Evaluation of the Effect of the AmnioFix Amniotic Membrane Allograft in Patients Undergoing Posterior Instrumentation (NCT01357187) · Clinical Trials Directory