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Topical Finasteride vs Minoxidil for Androgenetic Alopecia

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What is being tested

topical finasteride

+ Topical minoxidil

Drug
Who is being recruted

Alopecia+4

+ Hair Diseases

+ Hypotrichosis

From 20 to 50 Years
+13 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 2
Interventional
Study Start: February 2025
See protocol details

Summary

Principal SponsorSheikh Zayed Medical College
Study ContactFarah Humera, post graduate resident derma
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2025

Actual date on which the first participant was enrolled.

This clinical trial aims to compare the effectiveness of two different topical treatments, finasteride and minoxidil, for addressing androgenetic alopecia, a common type of hair loss affecting both men and women. Traditionally, finasteride is taken orally to block a hormone linked to hair loss, but this study uses it as a topical spray to potentially minimize side effects by targeting the scalp directly. Minoxidil is another topical treatment that helps improve blood flow around hair follicles, encouraging hair growth. The study's goal is to explore which of these treatments is more effective in promoting hair growth, offering valuable insights for those struggling with hair loss. Participants in this study are divided into two groups, each consisting of 95 patients. One group receives a finasteride spray applied to the scalp twice a day, while the other group uses a minoxidil solution in the same manner. Both treatments continue for a period of 12 weeks. The results are evaluated after this period to assess the extent of hair growth improvement in each group. The study takes place in a hospital setting, ensuring that data is collected thoroughly and analyzed using statistical software, which helps in reaching reliable conclusions about the treatments' effectiveness.

Official TitleCOMPARISON OF EFFICACY OF TOPICAL FINESTERIDE VERSUS TOPICAL MINOXIDAL IN TREATMENT OF ANDROGENETIC ALOPECIA
NCT06826001
Principal SponsorSheikh Zayed Medical College
Study ContactFarah Humera, post graduate resident derma
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

190 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Male

Biological sex of participants that are eligible to enroll.

From 20 to 50 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

AlopeciaHair DiseasesHypotrichosisSkin DiseasesPathological Conditions, Signs and SymptomsSkin and Connective Tissue DiseasesPathological Conditions, Anatomical

Criteria

4 inclusion criteria required to participate
Age: 20-50 years

Patients not taking any treatment in last 1 month

Gender: Male

ANDROGENETIC ALOPECIA with AGA stage 2-6 Norwood-Hamilton -classification

9 exclusion criteria prevent from participating
Abrasion or abnormalities to the scalp

Hair transplant

Hypersensitivity

Recent history of local infections of the head

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Active Comparator
Group A will receive topical finasteride spray 0.25% twice daily for 12 weeks

Group II

Active Comparator
Group B will receive topical 5% minoxidil twice daily for 12 weeks

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Sheikh zayed Medical College and Hospital, Rahim Yar Khan, Punjab 644200

Rahim Yar Khan, PakistanOpen Sheikh zayed Medical College and Hospital, Rahim Yar Khan, Punjab 644200 in Google Maps
Recruiting soonOne Study Center
Topical Finasteride vs Minoxidil for Androgenetic Alopecia | PatLynk