PACTR201607001643276已完成未知
ow dose propofol versus lidocaine for relief of resistant post-extubation laryngospasm in the obstetric patient
Department of Anesthesia, Cairo University.0 个研究点目标入组 78 人开始时间: 2016年5月19日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 78
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
- 20 Year(s) 至 45 Year(s)(—)
- 性别
- Female
入选标准
- •All parturients of ASA class I or II, who were scheduled for cesarean section under general anesthesia, suffered from post-extubation laryngospasm.
排除标准
- •known sensitivity to lidocaine or propofol
- •upper respiratory tract infection
- •history of bronchial asthma or other lung diseases
- •chronic smoking
- •chronic exposure to smokers, dust or fumes.
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