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A Study on Oral Combination Therapy with Minoxidil and Finasteride for Androgenetic Alopecia

A Study on the Efficacy and Safety of an Oral Combination of Minoxidil and Finasteride for the Treatment of Androgenetic Alopecia in Men

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1051250069
Enrollment
Unknown
Registered
2025-07-14
Start date
2025-07-14
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

AGA

Interventions

None listed

Sponsors

Hiratyama Takashi
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria will be eligible for the study: Male patients aged 18 years or older who have been diagnosed with androgenetic alopecia classified as Norwood type II to V Individuals with the capacity to provide informed consent Individuals who receive a thorough explanation of the treatment along with the informed consent document and voluntarily provide written consent Individuals deemed by the attending physician to require the treatment

Exclusion criteria

Exclusion criteria: Patients who meet any of the following conditions will be excluded from the study: Individuals who use narcotics or stimulants Individuals with severe heart disease or poorly controlled hypertension Individuals with a history of hypersensitivity to minoxidil or finasteride Individuals deemed inappropriate by the attending physician

Design outcomes

Primary

MeasureTime frame
Photographic assessment of the scalp based on the Norwood classification Subjective evaluation using a self-administered questionnaire Interview and reporting of adverse effects (e.g., hypertrichosis, edema, headache, palpitations) Blood tests to monitor for adverse effects such as liver dysfunction

Secondary

MeasureTime frame
subjective symptoms, etc.

Contacts

Public ContactTakashi Hirayama

OSAKA UMEDA SHINSHI CLINIC

hirayama@gents-clinic.com+81-663730404

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026