Study on drug blood concentration, effectiveness, safety, and drug tolerance using residual samples of permission system and notification type antimicrobial drug
Not Applicable
Recruiting
- Conditions
- infectious disease
- Registration Number
- JPRN-UMIN000030456
- Lead Sponsor
- Keio University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 3250
Inclusion Criteria
Not provided
Exclusion Criteria
1.subject licensing system and notification system Patients with a history of allergy to antibiotic drugs 2.Patients who are clinically judged to be unlikely to expect the efficacy of this drug in infections caused by this drug insensitive pathogen or resistant strain 3.Other patients judged inappropriate as subject of this study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method