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Laser Therapy for Pediatric Burn Scars

A Controlled Trial Investigating the Use of Laser Therapy to Improve Pediatric Burn Scars.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02707627
Enrollment
20
Registered
2016-03-14
Start date
2016-10-31
Completion date
2021-01-31
Last updated
2021-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burns, Cicatrix, Hypertrophic

Keywords

Pediatric, Laser, Burn, Scar, Photothermolysis

Brief summary

A new era of outcomes for pediatric burn patients has begun as burn care continues to improve. Unfortunately, complete restoration of burn-injured skin may be limited by the development of hypertrophic scarring. Treatment with laser therapy is one of the newest forms of scar therapy available. Although laser therapy has only been adopted by burn clinicians within the last several years, early evidence suggests that it may offer significant benefits. Thus the aim of this study is to investigate the effectiveness of using laser therapy to treat hypertrophic burn scars in pediatric patients by using a comprehensive set of subjective and objective scar assessment tools.

Interventions

DEVICELaser Therapy

Laser therapy is a technology that can be used to treat hypertrophic burn scars.

Sponsors

The Hospital for Sick Children
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age 1-18 years at presentation 2. Patients with a hypertrophic burn scar that has been clinically diagnosed by a burn care specialist 3. Hypertrophic burn scar resulting from any etiology 4. Hypertrophic burn scar is ≥ 2 months post healing 5. Ability to complete English- language questionnaires

Exclusion criteria

1. Patients with concomitant skin disease (i.e. chronic skin conditions, herpes infection) 2. Patients with a history of keloid scarring 3. Patients who cannot tolerate the intravenous (IV) sedation used to perform laser therapy procedures 4. Patients who have had previous laser therapy procedures

Design outcomes

Primary

MeasureTime frameDescription
Vancouver Scar Scale ScoreBaseline (month 0) to month 12The Vancouver Scar Scale is composed of four subscales which include pigmentation (range: 0 - 3), vascularity (range: 0 - 3), pliability (range: 0 - 5), and height (range: 0 - 3). Total Vancouver Scar Scale score refers to the score obtained by summing the values from each subscale (range: 0 - 14) with higher scores indicating a worse scar.

Secondary

MeasureTime frameDescription
Patient and Observer Scar Assessment Scale ScoreBaseline (month 0) to month 12The Patient and Observer Scar Assessment Scale consists of two independent scales: 1) the patient scale (patient-reported), and 2) the observer scale (clinician-reported). Both the patient scale as well as the observer scale include a set of individual subscales that assess scar severity (range: 1 - 10) with higher scores indicating a worse scar.
Scar thicknessBaseline(month 0) to month 12Scar thickness measurements will be taken at five study visits over the course of one year and will be measured using ultrasonography.
Scar stiffness measured by the DermaLab Combo® skin analysis deviceBaseline(month 0) to month 12Scar stiffness measurements will be taken at five study visits over the course of one year and will be measured using the DermaLab Combo® skin analysis device (Cortex Technologies, Hadsund, DK).
Scar stiffness measured by ultrasound elastographgyBaseline(month 0) to month 12Scar stiffness measurements will be taken at five study visits over the course of one year and will be measured using ultrasound elastography.
Scar colourBaseline(month 0) to month 12Scar colour measurements will be taken at five study visits over the course of one year and will be measured using the DermaLab Combo® skin analysis device (Cortex Technologies, Hadsund, DK)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026