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临床试验/NCT01212536
NCT01212536已完成不适用

Randomised Controlled Trial of the Airtraq Optical Laryngoscope and Conventional Laryngoscopy in Children

University Hospitals Bristol and Weston NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2010年8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
60
试验地点
1
主要终点
time taken to successful intubation

研究概览

简要总结

The investigators aim to compare the new paediatric Airtraq indirect optical laryngoscope with conventional direct laryngoscopy for tracheal intubation in a randomised crossover study during routine anaesthesia. The investigators hypothesise that the Airtraq is as good as conventional laryngoscopy for tracheal intubation of infants and children. This will be an equivalence rather than a non-inferiority study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
None

入排标准

年龄范围
— 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • All children less than 6 years of age, in whom a size 2.5 - 5.5 tracheal tube would be considered suitable.
  • Classified by the American Society of Anesthesiology (ASA) as grade 1-
  • Scheduled for surgery under general anaesthesia, and in whom tracheal intubation and neuromuscular blocking drugs are planned to be used.

排除标准

  • inability of patient or parents to understand the study or consent process
  • known or suspected difficult airway
  • ASA 4 and above

研究组 & 干预措施

Conventional

No Intervention

conventional laryngoscopy for intubation

Airtraq

Experimental

laryngoscopy with Airtraq for intubation

干预措施: Airtraq laryngoscopy (Device)

结局指标

主要结局

time taken to successful intubation

时间窗: 30 mins

The primary outcome measure will be time taken to successful intubation. This will be recorded by a second operator using a handheld stopwatch or wall clock with second hand. Time will commence when the intubation device is handed to the anaesthetist, and stopped after the first successful inflation of the lungs (first upstroke of capnography trace).

次要结局

  • Grade of laryngoscopy(30 mins)
  • POGO score(30 mins)
  • VAS ease of intubation(30 mins)
  • evidence of traumatic intubation(24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Michelle White

Consultant in Paediatric Anaesthesia and Critical Care

University Hospitals Bristol and Weston NHS Foundation Trust

研究点 (1)

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