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Can early intervention with CO2 laser therapy promote scar maturation following a burn injury?

Can early intervention with CO2 laser therapy promote scar maturation following a burn injury?

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000343404
Acronym
N/A
Enrollment
20
Registered
2016-03-16
Start date
2016-04-04
Completion date
2017-04-03
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

In high income countries, improvements in first aid and acute specialised care have resulted in reduced mortality from major burn injuries (from approximately 25% to less than 9%). Although specialised care has significantly improved outcomes for these patients, the near universal complication of burn-related scarring persists as a constant reminder of limitations of care. For burn survivors, the development of painful, restrictive and disfiguring scarring, known as hypertrophic scarring (HS), has an incidence ranging from 30-70% in reviewed epidemiological data. The treatment of scarring has, thus far, been unable to keep pace with the advancements in resuscitation and other acute therapies. The consequences of scar formation are many and varied, including joint contractures and stiffness, chronic pain, itching, and anhydrosis. Additionally, the emotional repercussions can be significant, with many patients reporting stigmatization and discrimination due to their burn scars. As the mortality of acute burn injury continues to diminish, the burden of scarring may continue to rise. Current treatment options for hypertrophic scarring are not yet sufficient to significantly reduce its associated morbidity. Burn clinicians and researchers are focused on understanding scarring in more depth and discovering potential ways to improve patient outcomes. Within this field of innovation, laser resurfacing techniques are gaining greater interest and are currently being utilised in several centres worldwide for the treatment of HS. The aim of this study is to investigate if the early use of laser treatment helps minimise scar, decreases the time required in pressure garments, improves range of motion and thus results in fewer episodes of expensive reconstructive surgery. A 10,600nm fractional carbon dioxide laser supplied by Lumenis Ltd is the device to be used in this study. This laser has FDA approval for over 100 applications including the management of scars. It has the ability to deliver precise high energy in short-pulses to thickened scars, and has a good record for safety and outcomes. The Burns Service of WA has been using this laser for over 18 months for the management of scars, and the health professionals involved have received the appropriate safety training. Participants will receive 3 laser treatments 4-6 weeks apart. Outcome measures will be conducted before laser treatment, after the last treatment of laser and 3 months post laser treatment.

Interventions

A 10,600nm fractional carbon dioxide laser supplied by Lumenis Ltd is the device to be used in this study. This laser has FDA approval for over 100 applications including the management of scars. It has the ability to deliver precise high energy in short-pulses to thickened scars, and has a good record for safety and outcomes. Participants will receive 3 laser treatments 4- 6 weeks apart. The timing of procedures is dependent on patient availability and availability of surgical capacity (ie spac

A 10,600nm fractional carbon dioxide laser supplied by Lumenis Ltd is the device to be used in this study. This laser has FDA approval for over 100 applications including the management of scars. It has the ability to deliver precise high energy in short-pulses to thickened scars, and has a good record for safety and outcomes. Participants will receive 3 laser treatments 4- 6 weeks apart. The timing of procedures is dependent on patient availability and availability of surgical capacity (ie space on theatre list). Each treatment session lasts between 5 and 15 minutes, depending on the size treated. The patient will receive either a general or local anesthetic prior to the procedure. The choice of anesthetic is at the patient's discretion. The treatments are delivered in a laser safe environment - either in the operating theatre or the laser treatment room on the burns unit. The area to be treated is determined by the surgeon and the patient before the procedure. The laser treatment is delivered by the burn surgeon who is trained in the use of laser therapies and holds a current laser licence. Outcome measures will be conducted before laser treatment, after the third (last) treatment of laser and 3 months after the third laser treatment.

Sponsors

Prof Suzanne Rea
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adults > 18 years of age Two or more non-contiguous discrete burn areas Each burn > 1% TBSA Scars which would ordinarily be managed by pressure garments All patients to be at least 3 months from burn injury

Exclusion criteria

Pregnant or lactating females, Facial scars Keloid scars Inability to give informed consent Systemic glucocorticoid use

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026