MedPath

Efficacy of three methods in the treatment of androgenic alopecia

Phase 3
Conditions
Androgenic alopecia.
male-pattern baldness
Registration Number
IRCT138902081159N3
Lead Sponsor
Vice chancellor for research, Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
44
Inclusion Criteria

Inclusion Criteria:
Men with androgenic alopecia referred to Skin and Stem Cell Research Center Clinics who are not willing to do hair transplantation

Exclusion Criteria

1- History of allergy or sensitivity to finastride
2- Abnormal findings in physical examination or hormonal tests
3- History of taking finastride or other 5- alfa reductase inhibitors within last 12 months
4- History of taking antiandrogenic drugs or minoxidil application during past 6 months
5- Lack of cooperation of patients or unwilling for participating in the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hair diameter. Timepoint: Before intervention and every three months after intervention. Method of measurement: trichoscan.;Hair Density. Timepoint: Before intervention and every three months after intervention. Method of measurement: trichoscan.;Patient satisfaction. Timepoint: 3,6,9 and 12 months after treatment. Method of measurement: VAS(0-10).;Physician rating scale. Timepoint: 3,6,9 and 12 months after treatment. Method of measurement: 0-7.
Secondary Outcome Measures
NameTimeMethod
Side effects of treatment. Timepoint: 3, 6, 9 and 12 months after treatment. Method of measurement: check list.
© Copyright 2025. All Rights Reserved by MedPath