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临床试验/NCT00459797
NCT00459797已完成不适用

Comparison of Conventional GlideScope to Single-Use GlideScope Cobalt for Orotracheal Intubation

Lawson Health Research Institute2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2007年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
2
主要终点
Time to intubation (seconds)

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 conventional (reusable) GlideScope videolaryngoscope or the single-use GlideScope videolaryngoscope. 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
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any patient who is ≥ 18 yrs. coming for elective surgery.
  • Endotracheal tube is indicated for the procedure in the opinion of the attending anesthesiologist.
  • Any operator who has performed ≥ 10 GlideScope intubations.

排除标准

  • Any patient in whom the use of the GlideScope is contraindicated in the opinion of the attending anesthesiologist.
  • Any patient with cervical spine abnormalities.
  • Any patients with known or probable difficult airways (this rare occurrence is unlikely to be evenly distributed between the groups and could skew the data).
  • Any patient requiring rapid sequence induction.

结局指标

主要结局

Time to intubation (seconds)

时间窗: Immediate

次要结局

  • Ease of intubation(after intubation)
  • Number of intubation attempts per group(after intubation)
  • Incidence of trauma in each group(after intubation)
  • Number of failures to intubate per group(after intubation)
  • Use of external laryngeal pressure per group(after intubation)
  • Laryngoscopic grade distribution in each group(after intubation)

研究者

申办方类型
Other

研究点 (2)

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