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临床试验/NCT01163656
NCT01163656已完成不适用

A Prospective Comparison of the Glidescope Cobalt to Standard Direct Laryngoscopy in Infants

Children's Hospital of Philadelphia2 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2010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
66
试验地点
2
主要终点
Time to Tracheal Intubation

研究概览

简要总结

The investigators seek to prospectively compare intubation with the Glidescope Cobalt to Direct Laryngoscopy (DL) in infants.

详细描述

We seek to study the intubation characteristics of a new video laryngoscope, the Glidescope Cobalt in children less than or equal to 1 yr of age. This evaluation would provide insight as to the efficacy of this device in facilitating intubation in infants.

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
— 至 1 Year(Child)
性别
All
接受健康志愿者

入选标准

  • Scheduled to undergo elective surgery at CHOP
  • American Society of Anesthesiologists (ASA) Physical Status I or II
  • Anesthetic plan requiring tracheal intubation with a neuromuscular relaxant
  • Parental/guardian permission (informed consent). Subjects will be too young to understand the study procedures and therefore assent will not be sought. -

排除标准

  • At known or anticipated high risk for aspiration pneumonia
  • Known or predicted difficult intubation as assessed by the clinical attending anesthesiologist
  • Emergency surgical procedure
  • Patients with preoperative airway pathology or stridor -

结局指标

主要结局

Time to Tracheal Intubation

时间窗: Measured the time of the randomized device past the teeth/gums until its removal after intubation as the time to intubation.

The amount of time it takes the anesthesiologist to insert a breathing tube using one of two methods, either by direct laryngoscopy or using the Glidescope Cobalt Video system.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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