Overview

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

Status:
Withdrawn
Trial end date:
2018-08-01
Target enrollment:
0
Participant gender:
Female
Summary
The investigators propose to conduct a head-to-head, randomized clinical trial to compare the effectiveness of Minoxidil with Spironolactone and Finasteride in treating postmenopausal females with Androgenetic Alopecia (AGA).
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Florida
Treatments:
Finasteride
Minoxidil
Spironolactone
Criteria
Inclusion Criteria:

- female

- postmenopausal (>60 years old or with total hysterectomy)

- diagnosed with androgenetic alopecia

- no chemical processing or changes in hair products throughout the study

Exclusion Criteria:

- men

- premenopausal women (<60 or without hysterectomy)

- participants allergic to any of the study medications (minoxidil, finasteride,
spironolactone)

- participants with other co-existing forms of alopecia (traction, alopecia areata, or
scarring alopecias)

- participants with obstructive uropathy or advanced liver disease

- prior hair loss treatment within the last 6 months

- hair loss from the chemotherapy or other medication-induced alopecia

- Hair loss for greater than 5 years, as medical therapy is unlikely to have much effect
at restoring hair follicles inactive for that long of a period.