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临床试验/NL-OMON19993
NL-OMON19993已完成不适用

High-Flow Nasal Cannula for severe COVID-19, a multicentre prospective cohort study

o sponsors0 个研究点目标入组 600 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • The population included will be hospitalized patients with confirmed COVID-19, = 18 years old with isolated severe hypoxic respiratory failure defined as: SpO2 < 92% and/or BF>30/min despite treatment with at least 6 L/min oxygen therapy on nasal cannula. These patients may be included at the pulmonary departments delivering COVID-19 care, intensive care units or directly on the Emergency department. SARS-CoV-2 negative patients (nasopharyngeal PCR) will be excluded for this analysis, retrospectively.
  • Inclusion criteria
  • In order to be eligible to participate in this study, a subject must meet all of the following inclusion criteria:
  • ? Age = 18 years
  • ? Admitted to the hospital
  • ? Suspect of COVID-19 or nasopharyngeal swab PCR confirmed COVID-19
  • ? SpO2 < 92% and/ or breathing frequency >30/min despite at least 6L O2/min on nasal cannula.

排除标准

  • A potential subject who meets any of the following criteria will be excluded from participation in this study:
  • ? Reasons for direct intubation, as per local standard of clinical care.
  • ? Patient does not accept treatment with HFNC
  • ? Anatomic abnormalities (recent surgery of the face, nose, or airway) that preclude an appropriate-fitting nasal cannula

研究者

发起方
o sponsors

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