WithdrawnPhase 4NCT02483195

The Use of 5mg Finasteride Versus 200mg Spironolactone and Topical 5% Minoxidil in Treating Postmenopausal Female Androgenetic Alopecia

Studying Alopecia

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Key facts

Sponsor
University of Florida
Principal Investigator
Christina L. Mitchell, M.D., MD
University of Florida
Intervention
5% Minoxidil(drug)
Eligibility
60 years · FEMALE
Timeline
20162018

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT02483195 on ClinicalTrials.gov

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