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
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