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Topical treatment regimens in male androgenetic alopecia

Efficacy of Topical Minoxidil alone, Topical Finasteride alone and Topical Minoxidil - Finasteride combination in Male Androgenetic Alopecia - A Randomized Open-Label Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025390
Enrollment
60
Registered
2020-05-27
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L649- Androgenic alopecia, unspecified

Interventions

Intervention1: Topical Finasteride: Patient is instructed to apply 1 ml of Topical Finasteride 0.25% solution, prepared in alcohol base, over affected area of scalp twice daily, for 6 months. Control

Sponsors

Lady Hardinge Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All new male patients with clinically diagnosed androgenetic alopecia of grade III or higher (Modified Norwood Hamilton classification)

Exclusion criteria

Exclusion criteria: 1. Patients who have used any topical or systemic drugs in the past 6 months to promote hair growth 2. Patients with other scalp diseases that affect hair growth including seborrheic capitis 3. Patients with elevated levels of serum prostate specific antigen (PSA) 4. Patients with thyroid abnormality or vitamin D deficiency 5. Patients with history of continuing intake of following drugs â?? antihypertensives, antiepileptics, cytotoxic drugs, systemic corticosteroids, bronchodilators and vasodilators

Design outcomes

Primary

MeasureTime frame
Improvement in one or more of the following parameters in the three groups: 1. Mean Physician Assessment score (PAS) 2. Mean change in hair density from baseline 3. Mean change in number of terminal and vellus hair from baselineTimepoint: 12 and 24 weeks

Secondary

MeasureTime frame
Mean Patient Satisfaction Scores (PSS)Timepoint: 12 and 24 weeks;Proportion of patients experiencing side effects in the three groupsTimepoint: 12 and 24 weeks

Countries

India

Contacts

Public ContactDr Ram Chander

Lady Hardinge Medical College

chanderram41@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026