NCT00801047已完成4 期
Comparison of the Efficacy Intravenous Remifentanil PCA and Epidural PCEA for Labor Analgesia
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Primary analgesia end-point: VAS pain Score
研究概览
简要总结
Women requesting analgesia do not always wish to receive a potent analgesic method, and may fear the risks of epidural analgesia.
Study Aim: To determine whether remifentanil is effective for labor analgesia when compared with standard treatment (epidural analgesia).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
1
Experimental
Epidural group
干预措施: Bupivacaine epidural (Drug)
2
Active Comparator
Remifentanil iv PCA
干预措施: Remifentanil (Drug)
结局指标
主要结局
Primary analgesia end-point: VAS pain Score
时间窗: 1-6 hours
次要结局
未报告次要终点
研究者
研究点 (1)
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