CTRI/2013/12/004234已完成3 期
Does cuff pressure monitoring reduce post-operative pharyngo-laryngeal adverse events after LMA-ProSeal insertion? â?? A randomized trial
il0 个研究点目标入组 120 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 120
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
入选标准
- •adult patients (aged 18 to 80 years) with ASA physical status I, II and III scheduled to receive general anesthesia with LMA-ProSeal for short duration elective procedures like orthopedic, urologic and breast surgeries.
排除标准
- •any contraindication for the use of LMA (such as morbid obesity, gastro-esophageal reflux or previous upper abdominal surgery) or recent (within 7 days) history of upper respiratory tract infection.
研究者
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