Comparison of two different laser devices for axilla hair reduction.
Phase 3
- Conditions
- -.
- Registration Number
- IRCT2015010420514N2
- Lead Sponsor
- ational Institute for Medical Research Development (NIMAD)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
males or females with age of 18 – 50 years old; skin types II – IV; the subject must be willing to consent to participate in the study.
Exclusion criteria: children and pregnant or lactating women; any previous laser; treatment to the study areas; regional electrolysis within 6 months of study entry; history of keloid scarring; hormonal dysfunction; active cutaneous infection within the treatment area; chronic sun exposure or tanning; photosensitivity; use of medication with androgenic effects; history of skin pigmentation disorders; cancerous and pre-cancerous lesions in the treatment area; haired nevi in the treatment area; tattoos in the area to be treated.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The percentage of reduction of axilla hairs in both sides. Timepoint: Before treatment and 3, 6 and 12 months after last treatment. Method of measurement: Using before and after photos.
- Secondary Outcome Measures
Name Time Method Comparison of skin biophysical changes in both sides. Timepoint: Before treatment and 3, 6 and 12 months after last treatment. Method of measurement: Related probes of MPA device, CK electronic, Germany.;Comparison of pain level in both sides. Timepoint: Right after each treatment. Method of measurement: Visual analog scale (VAS).