NCT00636974已完成不适用
Minimum Local Anaesthetic Dose for Intrathecal Anaesthesia: a Randomised Comparison Between Levobupivacaine, Ropivacaine and Bupivacaine
Hospital Authority, Hong Kong1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2006年1月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 75
- 试验地点
- 1
- 主要终点
- Sensory block at 12th thoracic dermatome or above and successful conduct of the lower limb surgery up to 50 minutes after the intrathecal injection of the study drug
研究概览
简要总结
To determine and compare the effective intrathecal dose of levobupivacaine, ropivacaine and bupivacaine for 50% of patients in lower limb surgery
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
- Double
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •body weight=40-90kg,
- •height higher than 145cm
排除标准
- •Known hypersensitivity to amide local anaesthetics,
- •patients who do not understand English and Chinese,
- •Body mass index higher than 35 kg per sq metre
结局指标
主要结局
Sensory block at 12th thoracic dermatome or above and successful conduct of the lower limb surgery up to 50 minutes after the intrathecal injection of the study drug
时间窗: 50 minutes after the intrathecal injection of the study drug
次要结局
未报告次要终点
研究者
研究点 (1)
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