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N/A N=54 Randomized Single-blind Treatment

Effectiveness of Pressure Garment Therapy After Burns

Hypertrophic Scarring After Burn Injury

Enrolled (actual)
54
Serious AEs
0.0%
Results posted
Apr 2011
Primary outcome: Primary: Pressure Under Compression Garment — 25; 6.4 mm Hg

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Custom fabricated pressure garments (Device)
Age
Pediatric, Adult, Older Adult · 7+ yrs
Sex
All
Sponsor
University of Washington
Primary completion
Sep 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Pressure Under Compression Garment
25; 6.4
SECONDARY
Durometer (Hardness) of Wound
47; 46; 72; 39; 46; 49
SECONDARY
Color of Wound
56.3; 55.2; 9; 9.5; 8.2; 8.5
SECONDARY
Thickness of Wound
2.8; 3.4
SECONDARY
Clinical Appearance of Wound
3; 0; 38; 41
SECONDARY
Compliance With Wearing Compression Garment
20.4

Summary

Purpose - To determine the effectiveness of custom-fit pressure garment therapy in the prevention of hypertrophic scarring in healed burns. Background - Approximately one million people are burned each year in the United States. The most devastating outcomes following burns is the ugly, itchy, hypertrophic scar that interferes with work and all other aspects of life. Pressure garment therapy is routinely used to minimize hypertrophic scarring even though there is no scientifically valid data that this therapy is efficacious. Pressure garments are extremely unattractive, expensive and uncomfortable and their use needs to be based upon valid data. Goals and Objectives - The investigators plan to determine the effectiveness of pressure garment therapy in the control of hypertrophic scarring in healed burns. Methods - The I-Scan® device was designed to measure pressure at the body/environment interface and allows clinicians to deal with pressure-related problems for at-risk patients. It has been widely used in rehabilitation medicine but not with burn survivors. The investigators will use this device to measure the pressure at the garment/skin interface. 2) Furthermore, the few studies that have been attempted to determine efficacy have used between subjects designs. Since burn depth is extremely variable from patient to patient and since hypertrophic scarring is greatly influenced by age and race/origin, the between subjects design requires very large numbers of subjects. The investigators will use a within wounds design studying forearm burns and applying pressure to half of the wound and no pressure to the other half. The investigators will then compare hardness, color, thickness and clinical appearance.

Eligibility Criteria

Inclusion Criteria

  • Treated from time of burn at the University of Washington Burn Center during the first two years of the grant period
  • Burns covering the majority of the forearm that healed spontaneously in three or more weeks. Patients will be entered into the study within 4 weeks of injury.
  • Age 7-65 years. Patients younger than 7 years will be excluded given the cooperation required during follow-up evaluations. Patients over 65 years will be excluded since the incidence of hypertrophic scarring in persons over 65 is too low to warrant pressure garment trials.
  • Patients of any race, ethnicity, or skin color.
  • Informed, written consent in accord with the rules of the Human Subjects Committee of the University of Washington and the Health Insurance Portability and Accountability Act (HIPAA).

Exclusion Criteria

  • Incarcerated patients
  • Homeless patients
  • Patients with substance abuse
  • Patients with psychiatric diagnosis
  • Patients unavailable to return regularly for follow-up evaluations
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01005732). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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