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EFFICACY AND SAFETY OF TOPICAL FINASTERIDE 0.5% SOLUTION ONCE DAILY VERSUS TWICE DAILY IN THE TREATMENT OF MALE ANDROGENETIC ALOPECIA

Phase 2
Conditions
Male androgenetic alopecia aged 18-60 years
Male androgenetic alopecia, topical finasteride, videodermoscope
Registration Number
TCTR20240816002
Lead Sponsor
Faculty of Medicine, Srinakharinwirot University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending (Not yet recruiting)
Sex
Male
Target Recruitment
60
Inclusion Criteria

Male androgenetic alopecia aged 18-60 years Norwood-Hamilton classification type III vertex to V

Exclusion Criteria

1. History of male sexual problems
2. Underlying diseases of hepatitis, kidney disease, cardiovascular disease
3. History of depression, or suicidal idea
4. On the treatment of androgenetic alopecia within 6 months
4. Drug allergy to finasteride

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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