Pilot study to investigate the efficacy of rapamycin topical medicine against intractable hyperhidrosis
Not Applicable
Recruiting
- Conditions
- hyperhidrosis
- Registration Number
- JPRN-UMIN000015874
- Lead Sponsor
- Department of Dermatology Graduate School of Medicine, Osaka University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 3
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients who cannot carry out this treatment plan. 2) Patients who have allergy to macrolide antibiotics. 3) Patients who received oral or topical administration of rapamycin or RAD001 within 12 months prior to the study entry. 4) Patients who received topical treatment of aluminum chloride or iontophoresis within one months prior to the study entry. 5) Patients who received local injection of Botox within three months prior to the study entry. 6) Patients who received sympathectomy within 12 months prior to the study entry. 7) Patients during pregnancy or lactation 8) Patients who cannot undergo QSART and starch-iodine test 9) Patients who were judged unsuitable for this study by the investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method