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
- 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
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
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
Name Time Method 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
Name Time Method 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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