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Comparison of the effect of 0.5, 2.5 and 5 mg doses of oral minoxidil in the treatment of female pattern of hereditary hormonal hair loss

Phase 2
Recruiting
Conditions
Female pattern androgenic alopecia.
Androgenic alopecia
Registration Number
IRCT20220322054341N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients with clinical diagnosis of female pattern hair loss
Sinclair scale one to four
Age range 18 to 50 years old
Conscious consent to enter the study and the possibility of attending visits and follow-up sessions

Exclusion Criteria

Patients taking medication other than vitamins or minerals for alopecia
Pregnancy or breastfeeding
Patients with serious internal disease, especially heart disease or comorbidities at the treatment site
Psychiatric patients
Abnormal tests at baseline

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement rate. Timepoint: 3 and 6 months after starting treatment. Method of measurement: By sinclair scale, clinical and dermatoscopic images (Determine the number and thickness of hair shafts per square centimeter).
Secondary Outcome Measures
NameTimeMethod
Safety. Timepoint: 3 and 6 months after starting treatment. Method of measurement: Asking the patient about the side effects of treatment.;Tolerability. Timepoint: 3 and 6 months after starting treatment. Method of measurement: With Investigator Assessment of Tolerability scale (zero, low, medium and high or sufficient).;Patient satisfaction. Timepoint: 3 and 6 months after starting treatment. Method of measurement: With Caregiver treatment satisfaction (CTS) questionnaire (completely satisfied, satisfied, neither satisfied nor dissatisfied, dissatisfied and completely dissatisfied).
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