跳至主要内容
临床试验/NCT03171935
NCT03171935Unknown不适用

Wean Early With High-Flow Nasal Cannula Oxygenation Versus Noninvasive Positive Pressure Ventilation in Patients With Acute Hypoxemic Respiratory Failure: a Multicenter, Randomized, Controlled Trial (the WHEN Study)

Beijing Chao Yang Hospital1 个研究点 分布在 1 个国家目标入组 270 人开始时间: 2017年6月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
270
试验地点
1
主要终点
Duration of invasive mechanical ventilation

研究概览

简要总结

The main purpose of the present study is to verify whether, as compared with conventional weaning, early weaning with high-flow nasal cannula oxygenation or noninvasive positive pressure ventilation may more effective in shortening the duration of invasive ventilation, hence reducing the rates of complications and mortality in patients with acute hypoxemic respiratory failure.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Orotracheal intubation;
  • PaO2 <60mmHg(venturi mask,FiO2=0.5),and PaCO2 ≤45mmHg;
  • Meeting criteria for weaning readiness;
  • Spontaneous breathing trial failure.

排除标准

  • Duration of invasive ventilation <48h;
  • Tracheotomy;
  • Percentage of cuff leak volume in tidal volume<15.5%;
  • Unable to spontaneously clear secretions from their airway;
  • Recent oral,nasal,facial or cranial trauma or surgery;
  • Recent gastric or esophageal surgery;
  • Active upper gastro-intestinal bleeding;
  • Severe abdominal distension;
  • Lack of co-operation;
  • Chronic respiratory disease such as chronic obstructive pulmonary disease, asthma, interstitial lung disease and neuromuscular disease.

结局指标

主要结局

Duration of invasive mechanical ventilation

时间窗: 2.5 years

次要结局

未报告次要终点

研究者

发起方
Beijing Chao Yang Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zujin Luo

MD

Beijing Chao Yang Hospital

研究点 (1)

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