Clinical research evaluating efficiency of detection for antigen of tinea by trichophyton antigen kit in tinea pedis.
Not Applicable
- Conditions
- Tinea Pedis
- Registration Number
- JPRN-UMIN000038614
- Lead Sponsor
- Maruho Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who meet any of the following criteria will be excluded from the study. 1)Patients who has received oral antifungal drugs within 6 months(180 days) or patient who has received antifungal agent for external use within a month(30 days) prior to the enrolment. 2)Patients who participates in other clinical studies (except for observational study). 3)Patients determined to be inappropriate to be enrolled in this study by investigators.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method