JPRN-jRCTs061200052招募中未知
Clinical efficacy and safety of sitafloxacin for refractory urinary tract infection
Takehiro Iwata0 个研究点目标入组 92 人开始时间: 2021年2月2日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 92
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
- >= 20age old 至 ot applicable(—)
- 性别
- All
入选标准
- •Aged 20 years and over and fever >=37.5 degree centigrade with any urinary tract infection symptoms, such as costovertebral angel tenderness, micturition pain, urinary frequency, urgency or lower abdominal pain with pyuria. Pyuria was defined as: >=10 white blood cells (WBCs)/mL counted by flow cytometric analysis; >=10 WBCs/mm3 counted by counting chamber or a positive leucocyte esterase result using urine test paper with uncentrifuged urine; or .5 WBCs/high-power field in the sediment of centrifuged urine.
- •The patints who were diagnosed as complicated cystitis or recurrent cystitis or pyelonephritis or prostatitis or epididymitis.
排除标准
- •Patients who had a previous episode of quinolone hypersensitivity, who had allergic asthma or hives; immunosuppression; spastic diseases such as epilepsy; myasthenia gravis; aortic dissection; current pregnancy; renal failure, who are or will be pregnant.
- •Viable cell count before start of medication <10 ^ 5 CFU / mL.
- •Patients who have urethral catheterization or intermittent catheterization.
- •Patients who were judged as ineligible for this study by the investigators because of low compliance.
研究者
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