Osmidrosis treatment with percutaneous ethanol injectio
Phase 1
- Conditions
- Osmidrosis.Apocrine sweat disorders
- Registration Number
- IRCT2014122420426N1
- Lead Sponsor
- Vice Chancellor foer research of Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
having the complaint osmidrosis; age between 12-35 years old; both genders; willingness for participation in the study and signing the consent form. Exclusion criteria: pregnant or breast-feeding women; active infection at the axilla.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Osmidrosis. Timepoint: after ten months of injection. Method of measurement: starch-iodine test , visual analog scale(VAS).
- Secondary Outcome Measures
Name Time Method Patients satisfaction. Timepoint: At base line – at the end of the study. Method of measurement: visual analog scale (VAS).