Clinical Trial: Use of Amnion on Partial Thickness Burns
Study Status: Withdrawn
Recruit Status: Withdrawn
Study Type: Interventional
Official Title: Project Title The Treatment of Partial Thickness Burns: Treated Amnion Versus Currently in Use Topical Medications
Brief Summary: To determine if Amnion, used on partial thickness burn injuries would provide an improvement in rate of healing, pain control and scarring as compared to standard medical treatments.
Detailed Summary:
Sponsor: The University of Texas Medical Branch, Galveston
Current Primary Outcome: Length of time to 95% healing of treated burn wounds [ Time Frame: Assessment daily until 95 % healed ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
- Length of hospital stay [ Time Frame: Measured at hospital discharge ]
- Incidence of infection [ Time Frame: Measure daily until complete wound healing ]
- Amount of daily pain until wound is healed with different treatments. [ Time Frame: Daily until wound is completely healed. ]
- Amount of scaring with different treatments [ Time Frame: From injury to 2 years post burn ]
Original Secondary Outcome: Same as current
Information By: The University of Texas Medical Branch, Galveston
Dates:
Date Received: December 26, 2007
Date Started: June 2005
Date Completion:
Last Updated: November 13, 2012
Last Verified: November 2012
