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临床试验/NCT01235065
NCT01235065已完成不适用

GlideScope vs. Direct Laryngoscope for Emergency Intubation

University of Maryland, Baltimore2 个研究点 分布在 1 个国家目标入组 623 人开始时间: 2008年7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
623
试验地点
2
主要终点
Number of Participants Who Survived to Hospital Discharge

研究概览

简要总结

The purpose of this study is to assess if the GlideScope video laryngoscope is superior to the Macintosh direct laryngoscope for definitive airway management in acutely-injured patients.

详细描述

On admission to the emergency department following traumatic injury, many patients require placement of an artificial airway to support their breathing, provide oxygen and protect their airway. This procedure is accomplished through a number of different techniques and few studies have compared these techniques in order to establish the best method. We will compare an older technique using a metal handle and blade that allows for direct visualization of the vocal cords (direct laryngoscopy) to a newer technique that employs a fiberoptic bundle imbedded in a handle that allows indirect visualization of the vocal cords during placement of the artificial airway. The newer technique has the theoretical advantage of being more useful in patients with abnormal airways which are frequently encountered in trauma patients. Since both techniques are currently employed routinely in our institution, we will randomize all trauma admission to have an initial attempt with one of the two techniques in order to perform a randomized, unblinded trial.

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

  • require emergency intubation

排除标准

  • age < 18
  • require surgical airway on initial assessment
  • have known or strongly suspected spinal cord injury

结局指标

主要结局

Number of Participants Who Survived to Hospital Discharge

时间窗: 2 weeks, on average

Assessment of whether or not the patient was discharged alive from the study center

次要结局

  • Length of Time to Perform the Intubation Procedure(Up to 100 seconds)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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