跳至主要内容
临床试验/EUCTR2007-006198-98-NL
EUCTR2007-006198-98-NL进行中(未招募)不适用

Pain management in renal colic; The efficacy of continuous intravenous administration of tramadol versus butylscopolamine. A double blinded, randomized placebo controlled, prospective multicenter trial. - TraBu-trial

Isala klinieken Zwolle0 个研究点开始时间: 2009年9月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • The participants are 18 years and older and are able to make a will. Participants presenting with clinical signs and symptoms of renal colic, as ajudged by a urologist or resident in urology, are included after oral an written informed consent.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -pregnancy or lactation
  • -chronic tramadol use
  • -severe renal failure, GFR less than 10 ml/min
  • -severe hepatic failure
  • -allergic reactions to opioids / NSAID's
  • -concommitent use of MAO-inhibitor, or less than 2 weeks after stop MAO-inhibitor
  • -narrow-angle glaucoma
  • -use of NSAID's 8 hours before admittance
  • -use of drugs or alcohol 8 hours before admittance
  • -hydronephrotic kidney combined with fever

研究者

发起方
Isala klinieken Zwolle

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