The efficacy of a microwave device for treating axillary hyperhidrosis: Split-patient (1Pass vs 2Pass) comparative study
Not Applicable
- Conditions
- primary axillary hyperhidrosis
- Registration Number
- JPRN-UMIN000027772
- Lead Sponsor
- Tokyo Medical and Dental University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Secondary hyperhidrosis (2) Frey syndrome (3) Topical application of aluminum chloride within 4 weeks of consent acquisition (4) Local injection of botulinum toxin type A was conducted within one year of consent acquisition (5) Oral intake of anticholinergic drug within 2 weeks of acquiring consent (6) I underwent surgery on the axillary part (7) Serious underlying disease (history of xylocaine shock) (8) Diseases requiring systemic administration such as steroids (9) Systemic diseases such as collagen diseases that have impaired wound healing (10) any type of pacemaker implantation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of sweating amount by gravimetric method: amount of perspiration at 24 weeks after treatment between 1 or 2 pass groups
- Secondary Outcome Measures
Name Time Method