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Efficacy and Safety of Picosecond Laser versus Picosecond Laser Combined with Recombinant Humanized Type III Collagen for Melasma

Efficacy and Safety of Picosecond Laser versus Picosecond Laser Combined with Recombinant Humanized Type III Collagen for Melasma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113514
Enrollment
Unknown
Registered
2025-12-01
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

melasma

Interventions

Group A:picosecond laser, 3 treatments every 4 weeks for a total of 8 weeks. Parameters: Focus, DLA handset, spot 10mm, energy 0.21J/cm^2, frequency 10Hz, scan the lesion area 3-5 times, and the skin
Group B:Picosecond Laser Combined with Recombinant Humanized Collagen

Sponsors

Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Female patients aged 18-60 years; 2. Patients diagnosed with melasma and symmetrical distribution of the face, the course of the disease is at least 6 months; 3. The facial skin is basically intact, with no obvious inflammation, ulceration, exudation, etc.; 4. Those who have not received treatment (including laser and oral topical drugs) in the past 6 months; 5. Those who have no history of exposure to the sun in the past 3 months; Have good adherence and be able to participate in regular follow-up visits.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiovascular and cerebrovascular, liver and kidney and hematopoietic system and other systemic diseases, mental diseases, and immunodeficiency diseases; 2. Pregnant or lactating women; Those who are allergic to the test drug and its components; Females of childbearing potential on oral contraceptives and hormone replacement therapy; 3. Investigators who are participating in other clinical trials; 4. Those who, in the opinion of the investigator, are not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Melasma area severity index;

Secondary

MeasureTime frame
Physician’s overall assessment;Patient’s overall assessment;

Countries

China

Contacts

Public ContactFenglin Zhuo

Beijing Friendship Hospital, Capital Medical University

zflsunny@hotmail.com+86 159 1089 5068

Outcome results

None listed

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