Topical treatment for male hair loss using finasteride and minoxidil
Effectiveness and Safety of Topical Finasteride and Minoxidil Combination Compared to Topical Minoxidil for The Treatment of Male Androgenetic Alopecia
This study tests if using a mix of finasteride and minoxidil on the scalp can help men with hair loss grow more hair than just using minoxidil alone.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 59 Years |
| Sex | Male |
| Sponsor | Indonesia University Academic / other |
| Locations | 1 site (Jakarta, Other (Non U.s.)) |
| Trial ID | NCT05990400 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effectiveness and safety of a combination of topical finasteride and minoxidil compared to topical minoxidil alone in treating male androgenetic alopecia. It involves a double-blind, randomized, controlled design with 40 male participants diagnosed with androgenetic alopecia. The primary outcomes measured include hair density and hair diameter, assessed at baseline and every four weeks over a twelve-week period. Additionally, the study monitors any side effects associated with the treatments.
Who should consider this trial
Good fit: Ideal candidates for this study are males aged 18-59 diagnosed with androgenetic alopecia types III-V according to the Hamilton-Norwood criteria.
Not a fit: Patients with other scalp conditions, those using hair growth medications recently, or individuals with a history of adverse reactions to the study medications may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly improve hair growth and density in men suffering from androgenetic alopecia.
How similar studies have performed: Previous studies have shown promising results with similar combinations of topical treatments for hair loss, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Male aged from 18-59 years diagnosed with androgenic alopecia 2. Androgenic alopecia type III-V according to Hamilton-Norwood criteria 3. Willing to participate in this research by signing the consent form after receiving an explanation from the researcher 4. Willing to not cutting the hair nor coloring the hair during the study Exclusion Criteria: 1. Diagnosed with other infectious or inflammatory skin disease in the scalp 2. Using oral medications or vitamins that aim to increase the amount of hair in the last 1 month 3. Using topical medication that aim to increase the amount of hair in the last 2 weeks 4. Undergoing cosmetic procedure for AGA therapy such as low-level laser therapy (LLLT) procedures, platelet-rich plasma (PRP) injections, or microneedling within the last 3 months 5. Have sexual disorder such as decreased libido 6. Have a history of allergy or irritant contact dermatitis to the minoxidil and finasteride
Where this trial is running
Jakarta, Other (Non U.s.)
- University Indonesia — Jakarta, Other (Non U.s.), Indonesia (Recruiting)
Study contacts
- Study coordinator: Farah F Lubis, MD
- Email: farahfaulinlubis@gmail.com
- Phone: 081385088998
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.