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A double-blind split-face randomized controlled trial of the efficacy of 2% Curcuma aeruginosa Roxb. extract-containing cream compared with 2% ketoconazole cream in facial seborrheic dermatitis

Phase 3
Recruiting
Conditions
facial seborrheic dermatitis
facial seborrheic dermatitis, 2% Curcuma aeruginosa, 2% Ketoconazole
Registration Number
TCTR20210416002
Lead Sponsor
Research Administration Section, Faculty of Medicine, Thammasat University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
42
Inclusion Criteria

facial seborrheic dermatitis

Exclusion Criteria

1. Subjects with any untreated or uncontrolled dermatitis on the face, 2. severe co-morbidity, 3. suspected allergy to any study medication, 4. pregnant and lactating women, 5. Subjects who used topical agents(except bland emollients) on the face < 2 weeks before study was initiated, 6. Subjects who had used systemic antifungal agents for > 1 month

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
severity of facial seborrheic dermatitis at 4 weeks scoring index
Secondary Outcome Measures
NameTimeMethod
skin hydration, sebum week 2, 4 corneometer, sebumeter
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