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NCT07018349

Low Dose Oral Minoxdil in Androgenic Alopecia

Not yet recruiting NA Last updated 12 June 2025
What this trial tests

NA trial testing 2.5% Oral minoxidil in Androgenetic Alopecia (AGA) in 76 participants. Not yet recruiting.

Timeline
15 June 2025
Primary endpoint
30 September 2025
20 October 2025

Quick facts

Lead sponsorJinnah Postgraduate Medical Centre
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment76
Start date15 June 2025
Primary completion30 September 2025
Estimated completion20 October 2025
Sites1 location across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

Jinnah Postgraduate Medical Centre — full company profile →

Who can join

Adults 18 to 65, any sex, with Androgenetic Alopecia (AGA). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In order to successfully treat androgenetic alopecia (AGA), this study compares the efficacy of low-dose oral minoxidil dosages of 0.25 mg and 1 mg. It addresses a critical gap in current research, as few studies have examined the relationship between low dosage and outcomes like hair diameter, density, patient satisfaction, and adverse effects, including hypertrichosis. Previous research suggests that low dose of oral minoxidil is a safe and well-tolerated option for hair loss, but the optimal dose for maximizing benefits while minimizing side effects remains unclear. This study aims to determine which dose offers the best balance of efficacy and safety for AGA patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Androgenetic Alopecia (AGA)

Currently open trials in the same condition.

Other Jinnah Postgraduate Medical Centre trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07018349.

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