跳至主要内容
临床试验/NCT01054183
NCT01054183已完成不适用

The Use of the GlideScope Ranger in Pediatric Critical Care Transport

Akron Children's Hospital1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2010年7月1日最近更新:
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
22
试验地点
1
主要终点
Percent of Participants With Successful 1st Intubation Attempt

研究概览

简要总结

This study seeks to assess the role of the GlideScope Ranger video laryngoscope in facilitating successful neonatal/pediatric intubation by pediatric critical care transport teams. The central hypothesis of this study is that the GlideScope Ranger video laryngoscope reduces the rates of failed intubation attempts by pediatric critical care transport teams. The aims of this project are designed to specifically: (1) Establish competencies for GlideScope Ranger video laryngoscopy-assisted intubation for pediatric and neonatal patients; and (2) Compare the intubation success rates for intubation using GlideScope Ranger video laryngoscopy and using conventional, direct laryngoscopy by pediatric and neonatal critical care transport teams.

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 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • age < 18 years
  • Presence of respiratory failure requiring tracheal intubation by the Critical Care Transport Team either at the referring institution or during the transport to the receiving institution
  • Ability of parent or legal guardian to provide written informed consent

排除标准

  • Patients 18+ years of age
  • Patient has a functioning tracheostomy
  • Patient does not require orotracheal intubation

研究组 & 干预措施

Intubation using GlideScope Ranger

Experimental

The study site has two critical care transport teams per shift and will, at shift change, assign intubation team A to use the GlideScope Ranger for all intubations on that day.

干预措施: GlideScope Ranger Intubation (Device)

intubation using direct laryngoscopy

Active Comparator

The study site has two critical care transport teams per shift and will, at shift change, assign intubation team B. Team B will do intubations using direct laryngoscopy only that day.

干预措施: Direct Laryngoscopy (Device)

结局指标

主要结局

Percent of Participants With Successful 1st Intubation Attempt

时间窗: 30 days

Percent of participants with successful 1st intubation attempt by group (GVL vs. DL)

Overall Successful Intubation Rate: GlideScope Video Laryngoscopy (GVL) vs. Direct Laryngoscopy (DL).

时间窗: 30 days; no long-term outcome measures were included

Overall successful intubation rate defined as all successful intubations (by type) divided by all attempts (by type).

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 (1)

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