JPRN-UMIN000005772招募中4 期
Clinical efficacy and safety of double dose (200 mg tid) CDTR-PI based on scoring system for adult acute pharyngotonsillitis - Clinical efficacy of double dose CDTR-PI for adult acute pharyngotonsillitis
research association of okayama clinican0 个研究点目标入组 100 人开始时间: 2011年7月1日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 16years-old 至 ot applicable(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •- 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
研究者
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