Evaluation of efficacy and safety of anti-fungal drug for treatment of oral candidiasis
Not Applicable
- Conditions
- oral candidiasis
- Registration Number
- JPRN-UMIN000002231
- Lead Sponsor
- Keio University School of medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 244
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Patient who has history for another anti-fungal drug usage within a week. (2) Patient who has severe liver dysfunction (3) Patient with pregnancy or brest-feeding (4) Patient who hope pregnancy during trial duration (5) Patient who is evaluated with unfitness by the physician (6) Patient who is taking contraindicational drug
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method