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Comparison of the effectiveness of topical minoxidl and cetirizine in androgenetic alopecia

Phase 3
Conditions
Androgenetic Alopecia.
Androgenic alopecia
Registration Number
IRCT20230308057655N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
62
Inclusion Criteria

All patient with androgenetic alopecia aged 18 to 50
Patient who are willing to participate in trial

Exclusion Criteria

Patient with other types of alopecia
Any serious systemic disease
Patient who have had a history of hair transplantation in the past
History of sensitivity to cetirizine and minoxidil
Systemic steroid use for more than 14 days in the last 2 monthes

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The increase in density and thickness of hair. Timepoint: before the start of treatment and 4 months after the start of treatment. Method of measurement: Trichogram and standard photography in 4 views.
Secondary Outcome Measures
NameTimeMethod
Patient satisfaction score, doctor satisfaction score. Timepoint: The beginning of the study and 4 months after the start of the study. Method of measurement: A 7-point questionnaire to check the level of patient and doctor satisfaction.
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