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Treatment of keratosis pilaris with combined salicylic acid, licochalcone A, and isobutylamido thiazolyl resorcinol: A single-blind randomized controlled study

Treatment of keratosis pilaris with combined salicylic acid, licochalcone A, and isobutylamido thiazolyl resorcinol: A single-blind randomized controlled study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250401001
Enrollment
28
Registered
2025-04-01
Start date
2023-07-03
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

Keratosis pilaris on the outer arms Atopic dermatitis, Erythema, Follicular hyperkeratosis, Hyperpigmentation, Roughness

Interventions

Applied combined salicylic acid, licochalcone A, and isobutylamido thiazolyl resorcinol to one arms twice daily for 12 weeks ,Applied 10% urea cream to the contralateral arm twice daily for 12 weeks
Experimental Drug,Active Comparator Drug
Trio agent ,Urea

Sponsors

Division of Dermatology, Department of medicine, Faculty of Medicine, Ramathibodi hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Participants diagnosed with keratosis pilaris (KP) on both arms 2. Participants must voluntarily agree to participate in the study by signing an informed consent form 3. Participants must discontinue the use of any topical or systemic treatments for KP, for example; keratolytics (e.g., urea, lactic acid, salicylic acid, etc.), retinoids and corticosteroids at least 4 weeks

Exclusion criteria

Exclusion criteria: 1. Participants with major underlying conditions 2. Pregnancy or lactation 3. Presence of active skin disorders at the study sites 4. Known hypersensitivity to salicylic acid, urea, or any ingredient in the study agent 5. Participants with a history of laser or intense pulsed light treatments for KP within 6 months prior to enrollment

Design outcomes

Primary

MeasureTime frame
Skin roughness Baseline, week 4, week 8, week 12 Antera 3D,Skin hyperpigmentation Baseline, week 4, week 8, week 12 Antera 3D,Skin erythema Baseline, week 4, week 8, week 12 Antera 3D

Secondary

MeasureTime frame
Improvement score Week 12 A 10-cm visual analog scale rated by a blinded physician and patients ,Favorable score Week 12 A 10-cm visual analog scale rated by patients

Countries

Thailand

Contacts

Public ContactVasanop Vachiramon

Faculty of Medicine, Ramathibodi hospital

vasanop@gmail.com0946369165

Outcome results

None listed

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