Clinical study on biliary infection therapy :A RCT on clinical efficacy of DRPM in biliary tract infection with IPM/CS as comparator
Phase 3
- Conditions
- Acute biliaring infection
- Registration Number
- JPRN-UMIN000003852
- Lead Sponsor
- Hiroshima university hospital Department of General Internal Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
1)History of hypersensitivity to DRPM 2)Serious complications 3)Serious cardiac disfunctions 4)Serious renal disfunctions 5)With CNS disorder 6)History of hypersensitivity to B-lactam antibiotics 7)Pregnant or lactating women and women who may be pregnant 8)MRSA infection 9)Judged by investigator not to be appropriate for inclusion in this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical effectiveness
- Secondary Outcome Measures
Name Time Method Clinical effectiveness at 3,7days Safety(moniterd clinical and laboratory evaluation)