NCT00890942已完成不适用
Efficacy of Intramuscular Naloxone 0.4mg. in Prophylaxis of Intrathecal
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- efficacy of intrathecal naloxone 0.4mg. in prophylaxis of intrathecal morphine induced pruritus after cesarean section
研究概览
简要总结
The purpose of this study is to determine whether intramuscular naloxone 0.4mg. is effective in prophylaxis of intrathecal morphine induced pruritus after cesarean section.
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
- Triple (Participant, Care Provider, Outcomes Assessor)
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
- •patient schedule for cesarean section ASA class 1
排除标准
- •have contraindication for spinal block
- •complicated pregnancy
- •have history of drug abuse during pregnancy
- •obesity BMI>35kg./m2
研究组 & 干预措施
naloxone
Experimental
干预措施: naloxone (Drug)
normal saline
Placebo Comparator
干预措施: normal saline (Drug)
结局指标
主要结局
efficacy of intrathecal naloxone 0.4mg. in prophylaxis of intrathecal morphine induced pruritus after cesarean section
时间窗: 24 hour
次要结局
未报告次要终点
研究者
研究点 (1)
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