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临床试验/ACTRN12613001264774
ACTRN12613001264774已完成未知

A comparative study of high flow humidified nasal cannula versus standardised oxygen therapy for adult patients who present to the emergency department in respiratory distress. Success will be determined by a decrease in respiratory rate by 20% by the end of the second hour from the time therapy was commenced.

erida Bell0 个研究点目标入组 100 人开始时间: 2013年11月18日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
100

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
盲法
Blinded (masking used)

入排标准

年龄范围
16 Years 至 110 Years(—)
性别
All

入选标准

  • Patients who are 16years and over who present with dyspnoea and a respiratory rate great or equal to 25 and oxygen saturations of less than or equal to 93% on room air to either Royal Prince Alfred ED or Canterbury Hospital ED

排除标准

  • 1. Patients presenting to the ED who require immediate BiPAP or intubation/ventilation
  • 2. Any patient under the age 16
  • 3. Patients who have received a trauma call; including facial trauma, chest trauma
  • 4. Patients with suspected spontaneous pneumothorax
  • 5. Patients who are unable to provide informed consent (cognitive impairment, intoxication from drugs and/or alcohol, intellectual disability, mental illness)

研究者

发起方
erida Bell

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