NCT01437462已完成4 期
Postoperative Pain After Propofol Sevoflurane Anaesthesia: a Prospective, Randomized, Single-blinded Trial
适应症
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 168
- 试验地点
- 2
- 主要终点
- Postoperative consumption of an opioid (oxycodone)
研究概览
简要总结
The impact of anaesthetic method (intravenous vs. inhalational) has been proposed, but not proven in a large-scale study. The researchers aim to provide an investigation that has sufficient power to clarify the potential effect of anaesthetic method on postoperative need of opioids. Sevoflurane and propofol will be compared.
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
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 69 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Age 18-69 years
- •Gender: female
- •ASA status 1-3
- •Laparoscopic hysterectomy
排除标准
- •Body Mass Index over 35
- •Diabetes mellitus
- •Liver disease
- •Allergies to pharmaceuticals used in the Study
- •Present use of opioids
结局指标
主要结局
Postoperative consumption of an opioid (oxycodone)
时间窗: 20 hours
The consumption of oxycodone will be monitored by recording the amount of the drug received via a commercially available patient controlled analgesia (PCA) pump.
次要结局
- NRS (numeral rating scale) of pain(20 hours)
研究者
Arvi Yli-Hankala
Professor
Tampere University Hospital
研究点 (2)
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