NCT02326753已完成不适用
Gender and Proper Size of Oropharyngeal Airway: Pilot Study
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 36
- 试验地点
- 1
- 主要终点
- the proportion of patients whose oropharyngeal airway is proper
研究概览
简要总结
The purpose of this study is to assess the adequacy of mask ventilation with the different sized-oropharyngeal airway.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •adult patients undergoing surgery that requires general anesthesia
排除标准
- •anticipated difficult intubation
- •patients without teeth or with loose teeth
- •cervical spine disease
- •body mass index over 35 kg/m2
- •pregnancy
研究组 & 干预措施
No. 7 oral airway
Experimental
干预措施: No. 7 oral airway (Device)
No. 8 oral airway
Experimental
干预措施: No. 8 oral airway (Device)
No. 9 oral airway
Active Comparator
干预措施: No. 9 oral airway (Device)
结局指标
主要结局
the proportion of patients whose oropharyngeal airway is proper
时间窗: up to 10 minutes after the start of anesthetic induction
The oropharyngeal airway will be inserted into the patient's mouth. Investigators will check the laryngeal view using fiberoptic bronchoscope and the adequacy of ventilation after the investigator ventilates the patient using the face mask. If both the laryngeal view and ventilation are appropriate, the size of oropharyngeal airway will be considered as the proper size for the patient.
次要结局
未报告次要终点
研究者
研究点 (1)
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