A Postmarket Randomized Study of the Treatment of Superficial Partial-Thickness Burns Using Two Dressings

Stopped early · Not applicable

Conditions studied: Burns

In brief

The purpose of this research study is to compare the rate of healing, the infection or complication rate, pain perception and scarring from burn injuries using two types of burn dressings.

Key facts

Study ID

NCT01067729

Run by

Aubrey Inc.

Starts

2009-11-01

Last updated by the study team

2015-01-26

Who can join

Age: 1 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Superficial partial thickness burns
• Two non-contiguous burn sites or the same approximate size/depth for comparison, OR
• One burn site large enough to accommodate both a 6" square AWBAT™ dressing and a 6 " square Biobrane® dressing
• Burn wounds measuring >2% - <40% TBSA
• Patient age: >1 - 70 years

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

• UC Irvine Burn Center — Irvine, California, United States
• University of Missouri Health Care — Columbia, Missouri, United States
• Shriners Hospitals for Children — Galveston, Texas, United States

Full record on ClinicalTrials.gov

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