UnknownNot Applicable

Multi-Center, Prospective, Randomized, Comparison of AWBAT™-D vs. Xeroform™ or Glucan II™ for Treatment of Donor Sites in Burn Surgery

United States60 participantsStarted 2009-08

Plain-language summary

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.

Who can participate

Age range18 Years – 70 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Burn wounds measuring 1% - 30% TBSA requiring skin grafting * Anterior bilateral donor sites of approximately the same size taken from the thighs or abdomen Exclusion Criteria: * 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

What they're measuring

• To compare the rate of healing of donor sites. • To compare patient reported perception of pain • To compare the potential clinical complication rates of: o non-adherence, o seroma o hematoma o infection

Timeframe: 2 year follow-up

Trial details

NCT IDNCT00964470

SponsorAubrey Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2010-12

Contact for this trial

Steven Moss

760-602-8300 smoss@aubreyinc.com

View on ClinicalTrials.gov More Treatment of Donor Site Burns trials