Skip to content

Efficacy of 578 nm copper bromide laser on scar prevention

Efficacy of 578 nm copper bromide laser on scar prevention: A Double-blinded Randomized Controlled Trial.

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250218018
Enrollment
32
Registered
2025-02-18
Start date
2025-02-16
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Progression of surgical cesarean section scar prevention Vancouver scar scale ,Cosmetic appearance scale ,Copper bromide laser,Cesarean section wound,scar

Interventions

spot size hand piece 10 mm , yellow light , Energy Fluence 8 J/cm2 , Off time 800 ms every 4 week total 3 times split-side wound,No intervention split-side wound
Experimental Device,No Intervention No treatment
copper bromide laser,No intervention

Sponsors

None listed

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Female volunteers, Thai nationality (2) Age 20-40 years (3) Have a cesarean section wound and can undergo laser surgery within 7 days after suturing (4) Fitzpatrick skin type III-IV (5) Willing to participate in the project

Exclusion criteria

Exclusion criteria: 1) The participants was unable to attend the follow-up appointment or was unable to attend the experiment throughout the research period. (2) The participants did not consent to participate in the research. (3) The participants did not understand Thai. (4) The participants received both topical medications to reduce scars, steroid injections to the wound after surgery, and oral steroids that affected the protection of the cesarean section wound. (5) The participants had a history of photodermatoses, eczema, infection. (6) The participants had a history of complications after copper bromide laser surgery. (7) The participants had more than 2 cesarean sections

Design outcomes

Primary

MeasureTime frame
scar prevention evaluation by physician Before intervention and every month after intervention ( at 4,8,12 week ) Vancouver scar scale

Secondary

MeasureTime frame
scar prevention evaluation by participants Before intervention and every month after intervention ( at 4,8,12 week ) Cosmetic appearance scale,Adverse effects every month after intervention ( at 4,8,12 week ) checklist

Countries

Thailand

Contacts

Public ContactSuphitsara Naphapunsakul

Dhurakij Pundit University

beautysuph@gmail.com0984947829

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026