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临床试验/ISRCTN75198618
ISRCTN75198618已完成不适用

Types of urethral catheter for reducing symptomatic urinary tract infections in hospitalised adults requiring short-term catheterisation: a randomised controlled trial

niversity of Aberdeen (UK)0 个研究点目标入组 5,700 人开始时间: 2007年1月26日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
5,700

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

性别
All

入选标准

  • 1. Adult patients (both males and females, more than or equal to 16 years of age)
  • 2. Requiring urethral catheterisation (expected to be required for a maximum of two weeks)
  • 3. Pre-selected units with a high volume of short-term catheterisation

排除标准

  • 1. Patients for whom urinary catheterisation is expected to be long-term (i.e. more than 14 days)
  • 2. Urological intervention or instrumentation within preceding seven days (e.g. catheterisation, cystoscopy, prostatic biopsy and nephrostomy insertion)
  • 3. Non-urethral catheterisation (e.g. suprapubic catheterisation)
  • 4. Known allergy to any of the following: latex, silver salts, hydrogel, silicone or nitrofurazone

研究者

发起方
niversity of Aberdeen (UK)

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