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Dual-Wavelength Laser Treatment for Stubborn Birthmarks: A Clinical Study

Clinical Study on the Treatment of Refractory Café-au-Lait Macules with Combined 755nm and 1064nm Q-Switched Lasers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107273
Enrollment
Unknown
Registered
2025-08-07
Start date
2025-08-07
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Caf-au-lait maeules

Interventions

treatment group:The treatment side will receive Q755nm laser first, and then Q1064nm laser treatment if the patient recurs. The control side pigmentation was directly treated with the Q1064nm laser

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients, 1-60 years old (including 1 and 60 years old), regardless of gender; 2. Patients who have received Q755/Q694/Q532nm laser treatment for 5 or more times before and have improved the area of skin lesions by less than 25%; The area of the skin lesion is not less than 2cm^2; 3. All patients undergo dermatoscopy to rule out other pigmented diseases, and patients with a clear diagnosis of coffee milk spots need to undergo skin biopsy if the dermatoscopy cannot confirm the diagnosis. 4. After fully understanding the treatment plan and risks, I voluntarily sign the informed consent form, and am willing to accept my own controlled trial, and cooperate with follow-up and skin biopsy.

Exclusion criteria

Exclusion criteria: 1. Pregnant women or women with pregnancy planning to prepare for pregnancy; 2. Allergic to surface disinfectants; 3. Patients with wounds on the face or epidermal rupture; 4. Patients with severe organic diseases or mental illnesses; 5. Patients who are participating in other clinical trials; 6. Subjects who have undergone laser or energy therapy, aesthetic surgery (e.g., fillers, injections, plastic surgery), and/or chemical ablative treatments in the past 1 year; 7. Subjects with a history of skin healing disorders or scarring; 8. Patients who have participated in or are participating in other drug or device clinical trials within 3 months; 9. Patients with other conditions that the investigator believes are not suitable for participation in this clinical trial

Design outcomes

Primary

MeasureTime frame
Subjective Visual Assessment Score (VAS);

Secondary

MeasureTime frame
side effects;patient satisfaction;

Countries

China

Contacts

Public Contactzhen zhang

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

zz6503@vip.126.com+86 21 23271699

Outcome results

None listed

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