NCT01489605撤回不适用
Comparison of GlideScope Groove to Standard GlideScope for Orotracheal Intubation: A Non-inferiority Study
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 4
- 主要终点
- Duration of Intubation
研究概览
简要总结
Patients presenting for elective surgery requiring orotracheal intubation will be randomized to being intubated with either the GlideScope Groove video-laryngoscope or the standard GlideScope video-laryngoscope.
详细描述
See above. The primary outcome is time to intubation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Any adult patient booked for elective surgery requiring orotracheal intubation.
排除标准
- •Any patient with cervical spine abnormalities.
- •Any patients with known or probable difficult airways.
- •Any patient requiring rapid sequence induction.
研究组 & 干预措施
GlideScope Groove
Experimental
Patients will be intubated using the GlideScope Groove device. (Verathon)
干预措施: GlideScope Groove (Device)
Control: Standard GlideScope
Active Comparator
Control: Patients will be intubated using standard practice, a standard GlideScope (Verathon)
干预措施: Control: Standard GlideScope (Device)
结局指标
主要结局
Duration of Intubation
时间窗: Day 1
Duration of Intubation - Mask removal to ETCO2 confirmation
次要结局
- Sore Throat(Day 3)
- Incidence of trauma(Day 1)
- Ease of intubation(Day 1)
- Number of failures to intubate(Day 1)
- Use of external laryngeal pressure(Day 1)
- Laryngoscopic grade distribution(Day 1)
研究者
Timothy Turkstra
Staff Anesthesiologist and Associate Professor
Lawson Health Research Institute
研究点 (4)
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