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Use of Amnion on Partial Thickness Burns

NCT00674999 · Status: WITHDRAWN · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL

Last updated 2012-11-15

No results posted yet for this study

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.

Conditions

  • Burn

Interventions

BIOLOGICAL

Amnion

Application of Amnion with processing procedures involving the use of trypsin-EDTA

BIOLOGICAL

Amnion

Application of Amnion with processing procedures involving the use of Dispase II

DRUG

Polysporin/Bacitracin/Mycostatin

Application of Prepared antibiotic ointment: Polysporin, Bacitracin and Mycostatin combined

Sponsors & Collaborators

  • The University of Texas Medical Branch, Galveston

    lead OTHER

Principal Investigators

  • David N Herndon, MD · University of Texas

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-06-30
Primary Completion
2008-09-30
Completion
2008-09-30

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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 NCT00674999 on ClinicalTrials.gov