Comparative, double arm, non-randomized study for Androgenetic Alopecia.
Not Applicable
Completed
- Conditions
- Health Condition 1: L649- Androgenic alopecia, unspecified
- Registration Number
- CTRI/2022/05/042429
- Lead Sponsor
- A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10
Inclusion Criteria
Both Male and female patients with androgenic alopecia
Age 18 â?? 60 years.
Exclusion Criteria
Patients with other coexistent hair/scalp disorders (Alopecia Areata, trichotillomania, scarring alopecia etc.)
Patients on chemotherapy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hair density will be assessed and analysed with the help of trichoscan as well as global photographs by comparison between baseline and 16 weeksTimepoint: After 4 months
- Secondary Outcome Measures
Name Time Method Hair density will be assessed and analysed with the help of trichoscan as well as global photographs by comparison between baseline and 12 weeksTimepoint: After 4 months