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Comparison of the therapeutic effects of minoxidil solution alone with the combination of minoxidil and flutamide solution in patients with androgenic alopecia

Phase 3
Recruiting
Conditions
Androgenic alopecia.
Androgenic alopecia, unspecified
L64.9
Registration Number
IRCT20200825048515N6
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Confirmation of androgenic alopecia by two experienced dermatologists based on Hamilton diagnostic criteria
Patient consent to participate in the study
The intensity of hair loss in stage 2 to 5 according to Hamilton scale and in stages 1 and 2 according to Ludwig scale
The duration of hair loss is less than 10 years

Exclusion Criteria

History or observation of allergies to any of the drugs minoxidil and flutamide
History of heart disease and use of antihypertensive drugs
Receiving systemic treatment for androgenic alopecia during the 6 months prior to the study
Other types of alopecia such as alopecia areata, telogen effluvium, anagen effluvium and scarring alopecia of any systemic cutaneous disease

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hair density. Timepoint: Pre-and post-intervention. Method of measurement: Hair polarizer.;Severity of hair loss. Timepoint: Pre-and post-intervention. Method of measurement: By a skilled physician based on Hamilton-Norwood scale for male pattern hair loss and Ludwig scale for female pattern hair loss.
Secondary Outcome Measures
NameTimeMethod
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