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Clinical Trial 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.


Clinical Trial Description

The purpose of this study is to evaluate AWBAT™-D compared to Xeroform™ or Glucan II™ for the treatment of donor sites in burn surgery.

Primary Study Goals:

- To compare the rate of healing of donor sites.

- To compare patient reported perception of pain

- To compare the potential clinical complication rates of:

- non-adherence,

- seroma

- hematoma

- infection

Secondary Study Goal:

• To compare clinical outcome of donor sites: scarring based on the Vancouver Scar Scale. ;


Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00964470
Study type Interventional
Source Aubrey Inc.
Contact Steven Moss
Phone 760-602-8300
Email smoss@aubreyinc.com
Status Recruiting
Phase N/A
Start date August 2009