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临床试验/ACTRN12616001433493
ACTRN12616001433493已完成未知

THRIVE-F: Feasibility of THRIVE for improving the reliability of routine preoxygenation before induction of anaesthesia in children and adults undergoing surgery under general anaesthesia.

The University of Auckland0 个研究点目标入组 199 人开始时间: 2016年10月14日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
199

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment

入排标准

年龄范围
10 Years 至 o limit(—)
性别
All

入选标准

  • 1.aged 10 years or older
  • 2.having elective surgery under general anesthesia with intravenous induction in the study ORs with a participating anesthetist
  • 3.planned use of an endotracheal tube or a supraglottic airway device.
  • 4.scheduled start of anesthesia during working hours
  • 5.willing to provide informed consent

排除标准

  • 1.Known contraindication to Optiflow Trademark device
  • 2.Undergoing an operation on the acute list for which they have not been appropriately fasted
  • 3.More than 50% (as judged by the anesthetist) of the nares occluded by the nasal prongs
  • 4.Bleeding in nose or oropharynx
  • 5.Situations in which continuous positive airway pressure (CPAP) is contraindicated
  • 6.Pre-existing nasal obstruction
  • 7.Pre-existing hypoxemia

研究者

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