Safety and efficacy assessment of Alexandrite laser device in hair reductio
Phase 2
Recruiting
- Conditions
- unwanted hair.
- Registration Number
- IRCT20190210042676N15
- Lead Sponsor
- Parnian Gostar Parto Sanj
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Men and women aged 18 to 50 years
Skin type 1-4
Signing the consent form for participation in the study
Exclusion Criteria
History of using any type of laser hair removal in the treatment area in the last 12 weeks
If the percentage of white hair in the area is more than 5%
Pregnancy or lactating
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The rate of reduction of axilla hairs in both sides. Timepoint: Before treatment and 3 and 6 months after last treatment. Method of measurement: Trichoscopy By Fotofinder.
- Secondary Outcome Measures
Name Time Method Comparison of pain level in both sides. Timepoint: Right after each treatment. Method of measurement: Visual analog scale (VAS).