Topical AS101 for Treatment of FAGA (Female Androgenetic Alopecia) in Menopause Women
Phase 2
- Conditions
- Alopecia
- Registration Number
- NCT00418249
- Lead Sponsor
- Rabin Medical Center
- Brief Summary
The primary objective of this study is to assess the safety and efficacy of topical AS101 as treatment for Female Androgenetic Alopecia (FAGA) in menopause women.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 40
Inclusion Criteria
- Women in menopause, over 50 years of age.
- Clinically diagnosed for AGA, according to Ludwig scale I-II.
Exclusion Criteria
- Women treated with chronic medications.
- Use of Minoxidil within 3 months prior to entering study.
- Women who have underwent hair transplantation.
- Use of drugs with androgenic or anti-androgenic effects.
- Any other type of hair loss.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method hair density
- Secondary Outcome Measures
Name Time Method Self-administered satisfaction questionnaire Hair diameter, anagen/telogen ratio and hair growth rate,Global photographic assessment according to Female-Ludwig scale,
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie AS101's efficacy in treating Female Androgenetic Alopecia (FAGA)?
How does topical AS101 compare to minoxidil in managing hair loss in postmenopausal women?
Are there specific biomarkers that correlate with response to AS101 in androgenetic alopecia?
What are the potential adverse events associated with long-term AS101 topical application in menopausal patients?
What is the therapeutic potential of AS101 in combination with anti-androgens for FAGA treatment?