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Search / Trial NCT01005732

Effectiveness of Pressure Garment Therapy After Burns

Launched by UNIVERSITY OF WASHINGTON · Oct 30, 2009

Trial Information

Current as of July 22, 2025

Completed

Keywords

Hypertrophic Scar Burn Cicatrix Pressure Garment

ClinConnect Summary

No description provided

Gender

ALL

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

About University Of Washington

The University of Washington (UW) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a robust network of interdisciplinary teams, UW fosters collaboration among top-tier researchers, clinicians, and healthcare professionals, aiming to translate scientific discoveries into impactful treatments and interventions. The university is dedicated to ethical research practices and participant safety, ensuring rigorous adherence to regulatory standards in all clinical trials. Through its state-of-the-art facilities and extensive expertise, UW strives to address pressing health challenges and improve patient outcomes on a local and global scale.

Locations

Seattle, Washington, United States

Patients applied

0 patients applied

Trial Officials

Loren Engrav

Principal Investigator

University of Washington

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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