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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00969215
Other study ID # MF-02
Secondary ID
Status Completed
Phase N/A
First received August 29, 2009
Last updated July 24, 2011
Start date December 2009
Est. completion date December 2010

Study information

Verified date July 2011
Source Moy-Fincher Medical Group
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if fractional carbon dioxide laser treatment of a burn scar is a more effective method for improving the appearance of scars than the current available treatments.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 2010
Est. primary completion date September 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Have a mature burn scar and desire revision

- Fluent in English

- Must reside in the Los Angeles vicinity for the duration of the study

Exclusion Criteria:

- Previous history of scar revision

- Non-English speakers

- Pregnant or cognitively impaired subjects

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Lumenis fractional carbon dioxide laser
Laser resurfacing of a burn scar

Locations

Country Name City State
United States Moy-Fincher Medical Group Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
Moy-Fincher Medical Group

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evidence of clinical improvement of burn scar appearance as determined by blinded-observer and patient ratings. 2 weeks after each procedure No
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