JPRN-UMIN000010449已完成未知
Study of the clinical efficacy and number of days of administration of cefditoren pivoxil in the treatment of adult acute uncomplicated cystitis - Clinical efficacy of cefditoren pivoxil for adult cystitis
Okayama Urological Research Group0 个研究点目标入组 120 人开始时间: 2013年4月10日最近更新:
适应症
相关药物
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 120
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
- 20years-old 至 ot applicable（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •1) Co-presence of another urinary tract infection in addition to acute uncomplicated cystitis. 2) Symptoms of urinary tract infection within 4 weeks prior to onset of the present infection. 3) Existence of systemic (diabetes mellitus, ongoing administration of an immunosuppressive agent, ongoing long-term administration of steroid, etc.) or local factors that might induce and/or promote a urinary tract infection. 4) Symptoms/findings have improved as a result of administration of another antimicrobial agent. 5) History of allergy, possibly due to cephem antibiotics. 6) A physical constitution that predisposes to development of bronchial asthma, rash, urticaria or other allergic symptoms. 7) Moderate or more severe renal dysfunction. 8) Women who are or may be pregnant, are breast-feeding, or desire to become pregnant during the study drug administration period. 9) Any other reason that the chief investigator judges as rendering a patient inappropriate for enrollment.
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