IRCT201707157745N9已完成2 期
Comparative study of the duration of analgesia following spinal anesthesia with lidocaine 5% with fentanyl and marcain in pregnant women under cesarean section
Vice chancellor for research, YUMS0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- no limit 至 no limit（—）
- 性别
- Female
入选标准
- •Pregnant patients who come to the operating room for non-emergency c/s.
- •Exclusion criteria: patients with a history of diabetes, addiction, drugs are sedatives and psychoactive drugs.
排除标准
- 未提供
研究者
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