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Hypertrophic Scarring After Facial Burn
This study is currently recruiting participants.
Verified by Legacy Health System, April 2007
First Received: October 20, 2005   Last Updated: April 10, 2007   History of Changes
Sponsors and Collaborators: Legacy Health System
Total Contact
Information provided by: Legacy Health System
ClinicalTrials.gov Identifier: NCT00242970
  Purpose

Subjects with a burn to the face and/or neck will be enrolled into the study and a Three-Dimensional scanner used to see if it can objectively measure scar color and volume and measure the effect of scar on motion of the face and neck.


Condition Intervention Phase
Burn
Device: Cyberware 3030 RGB Color Scanner
Phase II

Study Type: Observational
Study Design: Screening, Longitudinal, Defined Population, Prospective Study
Official Title: Hypertrophic Scarring After Facial Burn: A Pilot, Observational Study of Static and Dynamic Measurements of Facial Scars With the 3-D Scanner Through the Scar Maturation Process

Resource links provided by NLM:


Further study details as provided by Legacy Health System:

Estimated Enrollment: 15
Study Start Date: October 2005
Estimated Study Completion Date: July 2008
Detailed Description:

Subjects will have 11 clinic visits over a 2-year period. An initial scan of the subject's head and neck will be made. Ten reproducible landmarks on the face and neck will be determined. The subject will return for follow up scans at Day 14, Day 28 and Month 2,6,9,12,18 and 24.

  Eligibility

Ages Eligible for Study:   4 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Face and/or Neck Burn
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00242970

Contacts
Contact: Lorraine Donison, RN 503 413-7945 ldonison@lhs.org

Locations
United States, Oregon
Legacy Emanuel Hospital and Health Center Recruiting
Portland, Oregon, United States, 97227
Principal Investigator: Helen Christians, OTR/L            
Sponsors and Collaborators
Legacy Health System
Total Contact
Investigators
Principal Investigator: Helen Christians, ORT/L Legacy Health System
  More Information

No publications provided

Study ID Numbers: OBC3DS-01
Study First Received: October 20, 2005
Last Updated: April 10, 2007
ClinicalTrials.gov Identifier: NCT00242970     History of Changes
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Burns
Hypertrophy
Facies
Wounds and Injuries
Disorders of Environmental Origin
Cicatrix

Additional relevant MeSH terms:
Burns
Wounds and Injuries
Disorders of Environmental Origin

ClinicalTrials.gov processed this record on September 10, 2009