Clinical Trials Directory

Trials / Terminated

TerminatedNCT01067729

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

A Multi-Center, Randomized, Prospective Study of the Treatment of Superficial Partial-Thickness Burns: AWBAT™ vs. Biobrane®

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
Sponsor
Aubrey Inc. · Industry
Sex
All
Age
1 Year – 70 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

The purpose of this study is to evaluate AWBAT™ compared to Biobrane® for the treatment of superficial partial-thickness burns using the patient as their own control.

Conditions

Interventions

TypeNameDescription
DEVICEAWBAT Wound Dressing
DEVICEAWBAT™, Biobrane®Comparison of burn dressings on randomized body sites using patient as own control

Timeline

Start date
2009-11-01
Primary completion
2011-06-01
First posted
2010-02-12
Last updated
2015-01-26

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01067729. Inclusion in this directory is not an endorsement.

A Postmarket Randomized Study of the Treatment of Superficial Partial-Thickness Burns Using Two Dressings (NCT01067729) · Clinical Trials Directory