Comparing the therapeutic efficacy of oral minoxidil and oral finasteride in androgenic alopecia in males
Pakistan naval ship Shifa hospital, Karachi
62 participants
Nov 3, 2025
Interventional
Conditions
Summary
A comparative study of oral minoxidil 1.25 mg daily with oral finasteride 1 mg on alternate days in androgenic alopecia, will be conducted at Dermatology out-patient department, PNS Shifa hospital Karachi after fulfilling the inclusion and exclusion criteria. After the informed written consent and permission from hospital’s ethics review committee, 62 patients will be divided in Group A & B. Patients in both the groups will receive treatment for 6 months and data from patient will be collected through a proforma on first visit and follow-ups', etc. The study aims to compare the effectiveness of two medications, oral minoxidil and oral finasteride, in treating androgenic alopecia (male pattern baldness).
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
Patients will be randomized into two groups (Group A&B). Group A will receive oral minoxidil 1.25mg daily ( Tab Minoxidil 2.5mg will be split into 2 halves and each half will be taken daily). All the patients will be provided with the same brand of medicine to minimize brand bias. All patients will asked to bring used tablet pack at every visit ( 1 visit per month) for adherence purposes.
Locations(1)
View Full Details on ANZCTR
For the most up-to-date information, visit the official listing.
ACTRN12625001306404