NCT00757198已完成4 期
Requirement of Analgesics After Two Remifentanil Dosing Regimen in Cardiac Surgery.
Kuopio University Hospital1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2008年9月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- Postoperative opioid (oxycodone) consumption
研究概览
简要总结
Prospective double blind study comparing two remifentanil dosing protocols (0.1 and 0.3 mcg/kg/min) during cardiac surgery. Main outcome measures are postoperative opioid requirements (PCA oxycodone) and postoperative pain (VAS, verbal rating scale).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Coronary artery bypass grafting patients
排除标准
- •Psychiatric disorders, sleep apnea, cardiac insufficiency
研究组 & 干预措施
1
Experimental
remifentanil o.1 mcg/kg/min
干预措施: remifentanil (Drug)
2
Active Comparator
remifentanil 0.3 mcg/kg/min
干预措施: remifentanil (Drug)
结局指标
主要结局
Postoperative opioid (oxycodone) consumption
时间窗: Postoperatively 48 hours
次要结局
未报告次要终点
研究者
Pasi Lahtinen
PhD,MD
Kuopio University Hospital
研究点 (1)
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