Clinical research evaluating efficiency of detection for antigen of tinea by trichophyton antigen kit in tinea unguium.
Not Applicable
- Conditions
- Tinea Unguium
- Registration Number
- JPRN-UMIN000038613
- Lead Sponsor
- Maruho Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 168
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 Concordance and discordance rates between the detection results of antigen of tinea by trichophyton antigen kit and the diagnosis of tinea unguium by KOH direct microscopy.
- Secondary Outcome Measures
Name Time Method