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Intradermal Botulinum Toxin A for Melasma: A Randomized Split-Face Study trial and in vitro study of its anti-melanogenic effect

Intradermal Botulinum Toxin A for Melasma: A Randomized Split-Face Study trial and in vitro study of its anti-melanogenic effect

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250118001
Enrollment
12
Registered
2025-01-18
Start date
2022-11-01
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

Melasma Melasma, Botulinum toxin, Pigment, Melanogenesis, UVA, Melanin, Tyrosinase

Interventions

Intradermal botulinum toxin injection,0.9%normal saline injection intradermally
Experimental Drug,Placebo Comparator Drug
Botulinum toxin,Normal saline

Sponsors

None listed

Eligibility

Sex/Gender
Female
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1.aged 20-55 years 2.Fitzpatrick skin types III and IV 3.patients had not received any melasma treatments (such as topical agents or light-based treatments) for at least one month prior to participation 4.any botulinum toxin (BoNT) injections were withheld for at least six months before the study

Exclusion criteria

Exclusion criteria: 1.pregnancy 2.lactation 3.use of exogenous hormones 4.thyroid disease 5.allergy or resistance to BoNT 6.bleeding disorders 7.neuromuscular disorders 8.active infections or skin diseases

Design outcomes

Primary

MeasureTime frame
Melasma Area and Severity Index score before, 2 wk, 1 mo, 2 mo, 3 mo Score,Physician global assessment score before, 2wk, 1mo, 2 mo, 3mo Score

Secondary

MeasureTime frame
Patient satisfaction 2wk, 1mo, 2mo, 3mo Score

Countries

Thailand

Contacts

Public ContactWilai Thanasarnaksorn

Samitivej sukhumvit hospital

dr.wilai@yahoo.com66829898923

Outcome results

None listed

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