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Evaluation of ACell Hydrated Wound Dressing for Autogenous Skin Donor Sites — ACell  

Burns Clinical Trial

Official title:
Evaluation of ACell Hydrated Wound Dressing for Autogenous Skin Donor Sites

Clinical Trial 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 on consenting burn patients who require excision and grafting surgery for their burn wounds.

Hypothesis: The mean healing time for wounds treated with the ACell dressing will be less than the mean healing time for wounds treated with the Standard of Care dressing.

Clinical Trial 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 standard donor site dressing, which is currently Xeroform. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00352729
Study type Interventional
Source United States Army Institute of Surgical Research
Contact
Status Withdrawn
Phase N/A
Start date November 2006
Completion date August 2007
View Details
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