Skip to content

Efficacy of infraorbital darkening treatment using multi-pulsed Q-switched 1064-nm Nd:YAG laser

Efficacy of infraorbital darkening treatment using multi-pulsed Q-switched 1064-nm Nd:YAG laser

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230821003
Enrollment
15
Registered
2023-08-21
Start date
2023-09-01
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

Patients with a history of infraorbital darkening diagnosed by dermatologist at least 1 year Infraorbital darkening, Q-switched 1064-nm Nd:YAG laser, fractional Q-switched laser, neocollagenesis, infraorbital rejuvenation, infraorbital volume

Interventions

Q-switched NdYAG laser have specific wavelength targeting on melanosomes, narrow pulse width of nanosecond and low fluence adjustment, the QSNYL with its selective photothermolysis and photomechanic
Experimental Device
multi-pulsed Q-switched 1064-nm Nd:YAG laser

Sponsors

none
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: - Healthy patient with a history of infraorbital darkening diagnosed by dermatologist at least 1 year - Fitzpatrick skin type II to IV

Exclusion criteria

Exclusion criteria: - Signs of active infection or inflammation around the eyes - Diseases related to infraorbital darkening - Active systemic severe medical diseases/ photosensitivity such as liver cirrhosis, thalassemia, systemic lupus erythematosus and dermatomyositis - Drug-induced hyperpigmentation such as hydroxychloroquine, chloroquine, gold or zidovudine - History of any ocular or periocular surgery e.g. blepharoplasty or treatment of fat herniation - History of abnormal wound healing process such as poor controlled diabetes mellitus or smoking - History of atopy - Pregnancy and lactation - Immunocompromised host/status - Sleep disorders such as sleep disturbance or narcolepsy - Use of oral retinoids within 6 months - Use of nonsteroidal antiinflammatory drugs, steroids, anticoagulants, blood thinning agents and topical whitening agents within 1 months. - Previous laser treatment, chemical peels or transepidermal whitening agents within 3 months

Design outcomes

Primary

MeasureTime frame
skin lightness baseline, 1 month after final session of laser Chromameter

Secondary

MeasureTime frame
Infraorbital volume baseline, 1 month after final session of laser Croma infraorbital hollow assessment ,Elevation and depression volume baseline, 1 month after final session of laser Antera 3D,skin color (red,blue,green) baseline, 1 month after final session of laser Chromameter,Improvement scale 1 month after final session of laser 6-graded improvement scale (deteriorating, worsening, neutral, no improvement, poor, fair, good, and excellent),Patient's satisfaction score 1 month after final session of laser 4-point scale (dissatisfied, fair slightly satisfied, intermediately satisfied, and very satisfied)

Countries

Thailand

Contacts

Public ContactMarisa Pongprutthipan

Faculty of Medicine, Chulalongkorn University

dr_marisa@yahoo.com66827814958

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026