Clinical investigation of the safety and effectiveness of Excilia Hair strengthening and ani hair loss Lotion in improving hair loss
Phase 2
Recruiting
- Conditions
- Hair loss.Nonscarring hair loss, unspecifiedL65.9
- Registration Number
- IRCT20210130050179N6
- Lead Sponsor
- Zist orchid pharmed Company
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 25
Inclusion Criteria
Male aged 18-55 years
General health
Hair Loss Status II, III, IV Based on Norwood Scale
Voluntary participation and signing written informed consent
Exclusion Criteria
Chronic active scalp disease other than hair loss
Using any prescribed drug or OTC for hair loss within the past 3 months
Documented sensitivity to formulation components
Any severe weight loss or strict diet therapy during the study
Oral or topical treatment of minoxidil within 6 months before entering the study.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Count changes in terminal hair. Timepoint: Before intervention, 8,16,24 and 32 weeks after the start of use. Method of measurement: Trichoscopy By Fotofinder device.
- Secondary Outcome Measures
Name Time Method Hair count changes. Timepoint: Before intervention, 8, 16 and 32 weeks after the start of use. Method of measurement: Trichoscopy By Fotofinder device.;Hair lost Changes, based on Global photographic review. Timepoint: Before intervention, 8, 16 and 32 weeks after the start of use. Method of measurement: One independent dermatologist will perform clinical assessments in a blinded fashion by scoring every photograph according to the Global photographic review scale.