Trials / Completed
CompletedNCT02088567
Amniotic Membrane in Total Knee Replacements to Reduce Scarring
A Prospective Randomized Clinical Trial Using Dehydrated Human Amnion/Chorion Membrane (dHACM) in Total Knee Replacement Patients to Reduce Post-operative Scarring.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 52 (actual)
- Sponsor
- MiMedx Group, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The overall objective of this study is to evaluate the effectiveness of dHACM in reducing scar tissue formation in total knee replacement patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Total Knee Arthroplasty | Total knee arthroplasty, per the usual practice of the physician. |
| OTHER | Application of dHACM | Application of dHACM at end of procedure before closing wound between the underlying fascia and the overlying skin layers to reduce scar formation |
Timeline
- Start date
- 2014-01-01
- Primary completion
- 2014-10-01
- Completion
- 2014-10-01
- First posted
- 2014-03-17
- Last updated
- 2015-09-23
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02088567. Inclusion in this directory is not an endorsement.