EUCTR2007-000351-33-SE进行中（未招募）不适用
Will paracetamol reduce the opioid requirements and the (opioid)related postoperative nausea?
Karolinska Universitetssjukhuset Solna0 个研究点目标入组 140 人开始时间: 2007年3月5日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 140
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
- Male
入选标准
- •140 patients , undergoing heart surgery will be randomised upon arrival to the intensive care unit to receive either paracetamol every 6th hour or placebo. 18 years and older.
- •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
- •Patients not suited for paracetamol. Non conversationable. Women.
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