Clinical efficacy and safety of double dose (200 mg tid) CDTR-PI based on scoring system for adult acute pharyngotonsillitis
Phase 4
Recruiting
- Conditions
- Adult pharyngitis and tonsillitis
- Registration Number
- JPRN-UMIN000005772
- Lead Sponsor
- research association of okayama clinican
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
- Cases with definite improvement of symptoms or observations by previous treatment of other antibiotics within 7 days before administration. - Cases of atypical infection caused by bacteria out of indication (eg. mycoplasma, chlamydia). - Cases with serious or progressive underlying disease/complication, hard to evaluate efficacy and safety. - Cases with severe renal function disorder (Ccr < 30 mL/min and/or on hemodialysis) - Cases with a history of hypersensitivity for cephalosporins and/or penicillins - Cases with concomitant use of other antibiotics (excluding the long-term, low dose macrolides therapy) - Other cases which doctor in charge decide that the patient is not suitable for the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical efficacy
- Secondary Outcome Measures
Name Time Method Safety