A randomized, placebo controlled trial comparing the efficacy of a combination of oral 5mg finasteride and 5% minoxidil solution versus 5%minoxidil alone in treatment of female pattern hair loss (FPHL) in post- menopausal women.

Phase 2

• Conditions: female pattern hair loss; Androgenetic alopecia; Female pattern hair loss; Finasteride; Post- menopausal women

• Registration Number: TCTR20170919003
• Lead Sponsor: none

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-09-19
• Study Completion: 2018-05-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

Female age 18-60
Menopause
History, clinical and dermoscope showed Ludwig classification I-4,II-1,II-2,frontal type

Exclusion Criteria

family history of breast cancer, thyroid disease, iron deficiency anemia, pregnancy, psychiatric problem, previous treatment with laser or medication within 3 months. previous hair transplant within 1 year

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
hair density at 24 weeks after start intervention hair density(non-vellus hair) at midscalp by Fotofinder®

Secondary Outcome Measures

Name	Time	Method
photographic assessment score at 24 weeks after start intervention photographic assessment questionaire,hair mass index at midscalp at start and 24 weeks after start intervention HairCheck® ,severity of female androgenetic alopecia at start and 24 weeks after start intervention Ludwig classification ,Satisfaction score at start and 24 weeks after start intervention patient self-assessment questionnaires,side effect 4 weeks after start intervention questionare