Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
ID01619917

The Role of Fractional Vascular Laser Therapy in the Management of Burn Scars

Led by University of Manitoba · Updated on 2026-05-14

6

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of fractional vascular laser therapy in managing burn scars, specifically focusing on how this treatment may improve scar height, texture, blood vessel appearance, and flexibility in mature burn scars. The study addresses the need for well-designed, randomized controlled trials since the current evidence for laser therapy's effectiveness in burn scar treatment is limited, and laser therapy can be costly compared to other options. Participants will receive fractional vascular laser treatment applied to one of two randomized scar locations: either proximal or distal to the heart. The laser treatment aims to remodel mature and inactive scars by resurfacing the skin and potentially reducing visible mesh patterns from skin grafts. The study involves a randomized, single-blind design comparing these two scar locations to assess the laser's impact. During the study, participants will be monitored every three weeks for up to 15 weeks to measure changes in the appearance of their burn scars. Researchers will assess scar features such as height, texture, vascularity, and pliability to determine the treatment's benefit. The total study period includes follow-up assessments to track scar improvement over time, ensuring detailed evaluation of the laser therapy's effects on late-stage burn scars.

CONDITIONS

Brief Title

The Role of Fractional Vascular Laser Therapy in the Management of Burn Scars

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Living in Winnipeg
  • Burn scar 6 to 12 months old
  • Fitzpatrick skin type I to III
  • Thermal burn scar on trunk or extremities
  • Age between 18 and 60 years
Not Eligible

You will not qualify if you...

  • Presence of an open wound

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Up to 15 weeks

Participants receive fractional vascular laser therapy applied to one scar site depending on randomization.

Visits every 3 weeks until Week 15

Trial Site Locations

Total: 1 location

1

University of Manitoba

Winnipeg, Manitoba, Canada, R3A 1R9

Actively Recruiting

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Research Team

J

Justin Gawaziuk, MSc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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