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
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