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Clinical Trials/NCT03171935
NCT03171935
Unknown
Not Applicable

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 site in 1 country270 target enrollmentJune 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patients With Acute Hypoxemic Respiratory Failure
Sponsor
Beijing Chao Yang Hospital
Enrollment
270
Locations
1
Primary Endpoint
Duration of invasive mechanical ventilation
Last Updated
4 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
June 1, 2017
End Date
March 31, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Beijing Chao Yang Hospital
Responsible Party
Principal Investigator
Principal Investigator

Zujin Luo

MD

Beijing Chao Yang Hospital

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Duration of invasive mechanical ventilation

Time Frame: 2.5 years

Study Sites (1)

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