High Flow Nasal Cannula Versus Non-Invasive Ventilation in Exacerbations of Chronic Obstructive Pulmonary Disease
Recruiting now · Not applicable
Conditions studied: Exacerbation Copd, Acute Respiratory Distress, Acute Hypercapnic Respiratory Failure
In brief
Chronic obstructive lung disease is a disabling disease that affects people usually after several years of smoke tobacco exposure and affects millions of patients worldwide. The disease is marked by multiples episode of worsening, termed exacerbations necessitating frequent hospitalizations. During these exacerbations, patients present breathless, and in the most severe cases, are admitted to an Intensive Care Unit (ICU) for respiratory assistance. Currently, respiratory assistance is provided by a ventilator via a oronasal mask (referred to non-invasive ventilation, NIV), that helps patients to cope with their breathless. The mask is not always well tolerated and the ventilator sessions are delivered intermittently. In the past decade, a new technique that provides air-oxygen with high flow has been developed. This technique, called High Flow via Nasal Cannula (HFNC) can deliver from 21 to 100% heated and humidified air-oxygen at a high flow of gas via simple nasal cannula. Recent studies have shown that the technique is very efficient to treat patients presenting with acute respiratory failure who don't have any underlying chronic pulmonary disease. Whether the technique would be also efficient in patients with COLD presenting with severe exacerbations has not yet been demonstrated. Since HFNC does not require any mask, it is thought that the comfort of the patient would be much better in comparison to NIV and could potentially help to treat many patients with the disease. The objective of the present study is to study the physiological effect of HFNC as compared to NIV in patients with severe exacerbations of COPD and to show that it is non-inferior to NIV.
Key facts
- Study ID
- NCT03033251
- Run by
- Unity Health Toronto
- People needed
- 30
- Starts
- 2018-09-02
- Expected to finish
- 2026-07-01
- Last updated by the study team
- 2025-05-20
Who can join
Age: 40 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- COPD exacerbation and acute hypercapnic respiratory failure with acute respiratory failure defined by
- Respiratory acidosis (pH ≤7.35 and PaCO2 ≥45 mmHg);
- Respiratory rate≥20 breaths/min;
- Activation of accessory respiratory muscles;
- Undergone at NIV or HFNC since their admission
- English speaking
- Adult patient with age > 40 year old.
You may not qualify if…
- Severe respiratory acidosis defined by pH<7.25
- Decreased level of consciousness (Glasgow Coma Score Scale < 11)
- Urgent intubation required
- Pneumothorax with pleural drainage and persistent air leak
- Hemodynamic instability requiring vasopressors
- Uncooperative
- Patients with skin or chest wall or abdominal trauma (potentially worsened by placement of a surface sensor)
- Clinical judgement of the attending physician
- Body mass index > 40 kg/m2
Where it is running
- St. Michael's Hospital — Toronto, Ontario, Canada (enrolling)
Full record on ClinicalTrials.gov
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