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Comparison of Skin Substitutes Used in Burn Care

NCT00676013 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 158

Last updated 2019-12-16

Study results available
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Summary

The purpose of this study is to determine if using a DERMAL LAYER under skin grafts:

1. will reduce scar formation of skin grafts
2. will reduce burn wound contractures
3. will improve functional outcome of joints requiring grafts

Compare scarring outcome of Dermal products

Conditions

  • Burns

Interventions

PROCEDURE

Integra

Grafting using the Commercial product Integra as a skin substitute over full thickness burn following excision.

PROCEDURE

AlloDerm

Grafting using the commercial product AlloDerm as a skin substitute

PROCEDURE

Homograft

Grafting using homograft as a skin substitute

PROCEDURE

Autograft

grafting using patients own skin from a separate donor site

Sponsors & Collaborators

  • The University of Texas Medical Branch, Galveston

    lead OTHER

Principal Investigators

  • David N Herndon, MD · University of Texas

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1997-12-31
Primary Completion
2011-01-31
Completion
2011-01-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT00676013 on ClinicalTrials.gov