NCT02745964终止不适用
A Comparison of LMA-Supreme and I-gel for the Incidence of Postoperative Sore Throat
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 8
- 试验地点
- 2
- 主要终点
- Postoperative sore throat
研究概览
简要总结
The purpose of this study is to investigate and compare the incidence of the postoperative sore throat between LMA supreme and I-gel.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 19 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •adult patients aged over 19 years who are scheduled for elective surgery under general anesthesia using the laryngeal mask airway
排除标准
- •Anticipated difficult airway
- •Expected duration of surgery more than 4 hours
- •body mass index more than 35 kg/m2
- •pregnancy
- •Upper gastrointestinal surgery or open abdominal surgery.
研究组 & 干预措施
LMA supreme
Experimental
Anesthesia is maintained using LMA supreme during surgery.
干预措施: LMA supreme (Device)
I-gel
Active Comparator
Anesthesia is maintained using I-gel during surgery.
干预措施: I-gel (Device)
结局指标
主要结局
Postoperative sore throat
时间窗: within 24 hours after the end of surgery.
The postoperative sore throat will be evaluated after the end of surgery by the investigator who are blinded to the group assignments. The investigator will ask the participant about his/her sore throat status.
次要结局
- Postoperative dysphagia(within 24 hours after the end of surgery)
- Postoperative dysphonia(within 24 hours after the end of surgery)
研究者
研究点 (2)
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