NL-OMON33885撤回4 期
Pain management in renal colic; The efficacy of continuous intravenous administration of tramadol versus butylscopolamine. A double blinded, randomized placebo controlled, prospective multicenter trial. - The efficacy of i.v administration of tramal versus buscopan in renal colic
Isala Klinieken0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 撤回
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Adults 18 years and older
- •Written and oral informed consent obtained
- •Mental capacity to make a will
排除标准
- •Pregnancy / lactation
- •Chronic tramadol use
- •Renal insufficiency, creatinine clearance < 10 ml/min
- •Hepatic insufficiency
- •Severe COPD / respiratory insufficiency
- •Intolerance to NSAID's and/or opioids
- •Monoamine oxidase inhibitors use, or within 2 weeks after withdrawal
- •Narrow-angle glaucoma
- •Intoxication with alcohol or other drugs
- •NSAID use < 8 hours before presentation
- •Hydronephrosis together with fever
研究者
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