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Ablative Fractional Laser Surgery Improving Sleep Quality in Adult hypertrophic scar patients: A Prospective Cohort Study

Clinical study of classification and risk assessment of scar diagnosis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035268
Enrollment
Unknown
Registered
2020-08-05
Start date
2017-03-04
Completion date
Unknown
Last updated
2020-08-10

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

Conditions

scar

Interventions

CO2 fractional laser:CO2 fractional laser
Conventional sugery:Conventional sugery

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: aged at least 18 years and whose time interval from burn to scar occurrence was less than one year were included.

Exclusion criteria

Exclusion criteria: We excluded pregnant or lactating women, patients with current or recent cancer, severe systemic disease or keloids, and patients who were in a poor condition and cannot tolerate surgery under regional or general anesthesia, or previous CO2-AFL surgery.

Design outcomes

Primary

MeasureTime frame
sleep quality;

Secondary

MeasureTime frame
itch;pain;

Countries

China

Contacts

Public ContactLv Kaiyang

Shanghai Changhai Hospital

lvkaiyng01@163.com+86 13816983691

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026