drugset / Trial / NCT07273799

Comparison of Outcomes Between Topical Minoxidil Versus Oral Minoxidil for the Treatment of Androgenetic Alopecia

NCT07273799

Phase 3 Not yet recruiting 200 enrolled Sheikh Zayed Federal Postgraduate Medical Institute
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To compare the outcome of topical minoxidil 5% spray versus oral minoxidil 2.5 mg tablet for the treatment of androgenetic alopecia in males and females. Outcomes include efficacy of the treatment, measured by reduction in hair shedding, improvement in hair density and new hair growth as assessed by physican and patient assessment as well as safety, defined as incidence and severity of adverse events over a treatment period of 6 months

Timeline

Start
2025-12-20
Primary completion
2026-05-01
Completion
2026-06-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Minoxidil Small molecule 2.5 mg Topical
Subject Minoxidil Small molecule 5 % Topical

Indications