comparitive study of two antifungal medicines in treatment of superficial fungal infectio
Not Applicable
- Conditions
- Health Condition 1: null- Fungal infected stable patients.
- Registration Number
- CTRI/2018/07/015063
- Lead Sponsor
- IMS BH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Tinea cruris
Tinea corporis
Tinea faciei
Exclusion Criteria
weight more than 80 kg
Any other co-morbidities like hepatic disorders, renal disorders, cardiac disorders, etc.
history of oral antifungal agents within one month of start of study.
pregnancy.
lactation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method