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A study comparing two laser treatments for improving facial melasma

A split-face comparative study of 1064 nm picosecond Nd:YAG laser versus 1064 nm picosecond Nd:YAG laser combined with 675 nm diode laser in the treatment of facial melasma. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096765
Enrollment
15
Registered
2025-11-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: L814- Other melanin hyperpigmentation

Interventions

Intervention1: Picosecond Nd:YAG (PSNY): On split-face Side A, Picosecond Nd:YAG (PSNY) laser toning monotherapy will be performed using a full-spot handpiece in non-contact mode, maintaining a 1–2 cm

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Male or female adult patients aged 18-85 years with Fitzpatrick skin types III-V affected by any type of facial melasma (epidermal, dermal, mixed, centrofacial, malar, or mandibular type).

Exclusion criteria

Exclusion criteria: 1.Photosensitivity 2.Active infection on the face 3.History of cutaneous malignancy 4.Immunosuppressed state 5.Use of topical retinoids within the previous 12 months 6.Laser procedure, peel, or dermabrasion within the previous 3 months 7.Use of topical lightening creams in the treatment area within the past 1 month 8.Pregnant or lactating 9.Unable to give informed consent

Design outcomes

Primary

MeasureTime frame
To assess the change in the Hemifacial-Modified Melasma Area and Severity Index (Hemi-mMASI) score from baseline to post-treatment follow-up.Timepoint: After 20months

Secondary

MeasureTime frame
compare clinical improvement in facial melasma using standardized photographs and evaluate pigment dilution through QuantifiCare LifeViz® Mini 3D imaging at baseline and at the end of the study (week 8). Changes in dermoscopic pigmentary and vascular component scores, patient satisfaction with the combined laser therapy, and any treatment-related adverse effects will also be assessed at every visitTimepoint: After 2 months

Countries

India

Contacts

Public ContactDr Chaithra Shenoy

CUTIS Academy of Cutaneous Sciences

chaithrashenoy@gmail.com9739247155

Outcome results

None listed

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