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临床试验/EUCTR2020-003682-19-BE
EUCTR2020-003682-19-BE进行中(未招募)1 期

Post-operative patient controlled intravenous oxyco-done vs patient controlled intrav nous piritramide. A randomized controlled trial.

Z Brussel0 个研究点目标入组 400 人开始时间: 2020年12月4日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
400

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

  • = 18 years
  • ASA class I, II or III
  • Abdominal or gynecological surgery (both open as laparoscopic)
  • 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 400
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • Patient has shown an oversensitivity to oxycodone or piritramide
  • Patients requiring urgent surgery (e.g. hemoperitoneum, bowel perforation, GI obstruction)
  • Disorders that might have an effect on perception of pain (e.g. fibromyalgia, psychiatric dis-orders)
  • Liver insufficiency
  • Renal insufficiency witch clearance < 10ml/min
  • Pregnancy / breast feeding
  • Patients enrolled in another study

研究者

发起方
Z Brussel

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