Status:
WITHDRAWN
Evaluation of ACell Hydrated Wound Dressing for Autogenous Skin Donor Sites
Lead Sponsor:
United States Army Institute of Surgical Research
Conditions:
Burns
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to see if treating a donor site wound with the ACell dressing is as good as or better than the dressings we currently treat harvested donor sites with. This will be tested...
Detailed Description
This is a single-center, prospective, randomized, and controlled study to evaluate the effectiveness of the ACell Dressing for use as a dressing for autogenous skin donor sites compared to our current...
Eligibility Criteria
Inclusion
- less than 30% total body surface area burn
- burn wounds do not involve the donor site harvesting areas
- requires excision and grafting of sufficient extent to justify two donor site of roughly equal size on non-dependent body surfaces.
- The scheduled excision and grafting procedure is the first such operation for the subject
- subject agrees to participate in follow-up evaluations
Exclusion
- Critical illnesses such as those requiring ventilator support, systemic infection, or hemodynamic instability
- Major acute or chronic medical illness that could affect wound healing
- Cellulitis or other infection of the potential donor sites
- Donor site has been previously harvested for grafting
- Subjects who are pregnant
- Religious objections or allergy to porcine products
Key Trial Info
Start Date :
November 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2007
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00352729
Start Date
November 1 2006
End Date
August 1 2007
Last Update
July 21 2015
Active Locations (1)
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1
U.S. Army Insitute of Surgical Research
Fort Sam Houston, Texas, United States, 78234