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Comparing the efficacy and safety of the combination of minoxidil 2.5 mg dutasteride 0.5 mg with minoxidil 2.5 mg and dutasteride 0.5 mg alone in the treatment of androgenic alopecia in men

Comparing the efficacy and safety of the combination of minoxidil 2.5 mg dutasteride 0.5 mg with minoxidil 2.5 mg and dutasteride 0.5 mg alone in the treatment of androgenic alopecia in men

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240304061159N1
Enrollment
45
Registered
2024-04-30
Start date
2024-04-27
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Androgenic Alopecia. Androgenic alopecia

Interventions

Intervention 1: Intervention group: In the first group, one third of the patients, which are estimated to be 15, are treated with 2.5 mg oral minoxidil tablets, 1 tablet per day for a period of 6 mont

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients aged 18 to 60 years with male androgenetic alopecia grade 2 to 4 vertex of Norwood-Hamilton classification who have not received any other medical treatment for hair loss in the last 6 months

Exclusion criteria

Exclusion criteria: Patients who are not diagnosed with androgenic alopecia or are being treated with other drugs, and patients with grade I of androgenic alopecia and patients with severe complications after taking drugs are excluded from the study. Liver and TSH tests (tests in the last 6 months can be it is accepted) it is requested that they will be excluded from the study in case of disorder. Patients with a history of hair transplantation and patients with prostate and breast cancer in the last 5 years will be excluded from the study. patients with a history of diseases related to the right ventricle and neurogenic hypotension And spinal injuries are not included in the study.

Design outcomes

Primary

MeasureTime frame
Counting the number and density of hair with Trichoscan. Timepoint: Before the start of the study and 2,4,6 months after the start of the intervention. Method of measurement: Trichoscan.

Secondary

MeasureTime frame
Comparison of hair changes and hair growth with photography. Timepoint: Before the start of the study and 2,4,6 months after the start of the intervention. Method of measurement: Photographic Examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Firooz

Tehran University of Medical Sciences

babakhanisina1@gmail.com+98 21 8897 2220

Outcome results

None listed

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