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The Pilot Study of the Efficacy and Safety of Using a 1726 nm Laser System for the Treatment of Xanthelasma in Thai Population.

The Pilot Study of the Efficacy and Safety of Using a 1726 nm Laser System for the Treatment of Xanthelasma in Thai Population.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250216008
Enrollment
20
Registered
2025-02-16
Start date
2024-01-02
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

Xanthelasma, Xanthelasma, 1726-nm laser

Interventions

Patients were treated with 1726 nm laser 3 sessions every 4 weeks. Then they were instructed to follow up at 1, 3, and 6 months after last treatment.
Experimental Device

Sponsors

Faculty of Medicine Siriraj hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Male or female age 18 years old and older 2. Have Xanthelasma on eyelids

Exclusion criteria

Exclusion criteria: 1. Patients who are pregnant, lactating, and postpartum within 1 year 2. Patients with history of Cushing syndrome or Ehlers-Danlos syndrome 3. Patients with other skin diseases, or having infection at the area of face 4. Immunocompromised patients 5. Patients with hypertrophic scar or keloid 6. Patients with photosensitivity disorder 7. Patients with cancers or skin cancers 8. Patients with mental disorders 9. Received laser treatment or botulinum toxin within the last 6 months before participating in the study 10. Received treatment with filler within 12 months 11. Patients using anticoagulants or antiplatelets

Design outcomes

Primary

MeasureTime frame
Global Aesthetic Improvement Scale (GAIS) baseline, 1 month after 1st treatment, 1 month after 2nd treatment and 1, 3, and 6 months after 3rd treatment, Physician

Secondary

MeasureTime frame
Patients improvement scale baseline, 1 month after 1st treatment, 1 month after 2nd treatment and 1, 3, and 6 months after 3rd treatment, Quartile scale,Physicians' improvement scale baseline, 1 month after 1st treatment, 1 month after 2nd treatment and 1, 3, and 6 months after 3rd treatment, Quartile scale,Safety baseline, 1 month after 1st treatment, 1 month after 2nd treatment and 1, 3, and 6 months after 3rd treatment, Adverse events

Countries

Thailand

Contacts

Public ContactWoraphong Manuskiatti

Faculty of Medicine Siriraj Hospital, Mahidol University

woraphong.man@mahidol.ac.th024197000

Outcome results

None listed

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