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A comparative study of the efficacy and side effects of topical 5% dapsone versus 2.5%benzoyl peroxide in the treatment of acne vulgaris

A comparative study of the efficacy and side effects of topical 5% dapsone versus 2.5%benzoyl peroxide in the treatment of acne vulgaris

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250908003
Enrollment
50
Registered
2025-09-08
Start date
2024-02-05
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

Male or female with mild to moderate acne aged more or equal to 18 years old. acne, benzoyl peroxide, topical treatment, dapsone, side effects

Interventions

Topical 5% dapsone apply on face twice daily.,Control arm was 2.5% benzoyl peroxide apply on face twice daily.
Experimental Drug,Active Comparator Drug
Topical 5% dapsone,2.5% benzoyl peroxide

Sponsors

Faculty of Medicine, Srinakarinwirot University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Healthy men and women 2. Age 18 years old and older 3. Mild to moderate acne according to Thai Clinical Practice Guideline for Acne

Exclusion criteria

Exclusion criteria: 1. Use of topical anti-inflammation or topical acne treatment in 4 weeks prior to study 2. Use of oral anti-inflammatory drugs or drugs that may effects acne 4 weeks prior to study 3. Use of oral retinoid within 3 months prior to the study 4. History of Dapsone and Sulfa drugs allergy 5. Pregnant or breastfeeding women 6. Use of high risk drug induced methemoglobinemia ex. sulfasalazine 7. Has dermatitis of other infections than acne at face 8. G6PD deficiency

Design outcomes

Primary

MeasureTime frame
inflammatory lesions reduction baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks, 12 weeks number of acne lesions

Secondary

MeasureTime frame
noninflammatory lesions reduction baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks, 12 weeks number of acne lesions,total lesion count baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks, 12 weeks number of acne lesions,GAAS score baseline, 2 weeks, 4 weeks, 6 weeks, 8 weeks, 12 weeks GAAS success rate,Side effects 2 weeks, 4 weeks, 6 weeks, 8 weeks, 12 weeks number of occurance,patient satisfaction score 12 weeks visual analog scale

Countries

Thailand

Contacts

Public ContactPinthisa Nisagornsen

Srinakharinwirot University

pinthisa.nis@gmail.com0851217776

Outcome results

None listed

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