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

NCT01067729 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL

Last updated 2015-01-26

No results posted yet for this study

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.

Conditions

  • Burns

Interventions

DEVICE

AWBAT Wound Dressing

DEVICE

AWBAT™, Biobrane®

Comparison of burn dressings on randomized body sites using patient as own control

Sponsors & Collaborators

  • Aubrey Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
1 Year
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2011-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01067729 on ClinicalTrials.gov