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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01619917
Other study ID # B2011: 075
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2012
Est. completion date July 1, 2026

Study information

Verified date November 2023
Source University of Manitoba
Contact Justin Gawaziuk, MSc
Phone 2047893669
Email jgawaziuk@hsc.mb.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

While the literature tends to support the use of laser therapy in the management of burn scars, there is a definite lack of appropriately powered, randomized controlled trials. Laser therapy can be quite expensive when compared to other treatment modalities for burn scars, and while promising, its true usefulness has yet to be conclusively demonstrated. For this reason, our assessing the effects of fractional vascular lasers on burn scars. It has been hypothesized that the fractional vascular lasers work on mature scars to decrease scar formation, and the fractional laser works on scar that is quiescent to promote remodelling. The retexturing/ resurfacing of the laser theoretically can decrease the visibility of the mesh pattern created by meshed split thickness skin graft). Objective: To determine the benefit of fractional vascular laser treatment in improving burn scar height, texture, vascularity and pliability in late burn scars.


Recruitment information / eligibility

Status Recruiting
Enrollment 6
Est. completion date July 1, 2026
Est. primary completion date June 1, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - living in Winnipeg - burn scar 6-12 months old - Fitzpatrick skin type I-III - thermal burn scar on trunk or extremities Exclusion Criteria: - open wound

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Fractional Vascular Laser
laser energy will be applied to one of 2 sites (proximal or distal) depending on randomization result

Locations

Country Name City State
Canada University of Manitoba Winnipeg Manitoba

Sponsors (1)

Lead Sponsor Collaborator
University of Manitoba

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary reduction in scar appearance examine with modified Vancouver Scar Scale every 3 weeks to 15 weeks
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