Multi-Center, Prospective, Randomized, Comparison of AWBAT™-D vs. Xeroform™ or Glucan II™ for Treatment of Donor Sites in Burn Surgery
Status unconfirmed · Not applicable
Conditions studied: Treatment of Donor Site Burns
In brief
The purpose of this study is to compare the rate of healing and the non-adherence of three types of dressings. The study will also compare rate of infection, scarring and perception of pain associated with treatment.
Key facts
- Study ID
- NCT00964470
- Run by
- Aubrey Inc.
- People needed
- 60
- Starts
- 2009-08-01
- Last updated by the study team
- 2010-06-22
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Burn wounds measuring 1% - 30% TBSA requiring skin grafting
- Anterior bilateral donor sites of approximately the same size taken from the thighs or abdomen
You may not qualify if…
- Ventilator dependence
- Pregnancy /Lactation
- Mechanism of injury was electrical, chemical or frostbite
- Co-morbidity which may compromise healing
- Known allergy to porcine or porcine products
Where it is running
- Wishard Health Services Burn Center — Indianapolis, Indiana, United States (enrolling)
- The University Hospital Burn Center Cincinnati — Cincinnati, Ohio, United States (enrolling)
- Firefighter's Regional Burn Center — Memphis, Tennessee, United States (enrolling)
Full record on ClinicalTrials.gov
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