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临床试验/JPRN-jRCTs061200052
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

发起方
Takehiro Iwata

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