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High Flow Nasal Cannula vs Low Flow Oxygen for Respiratory Failure

N/A
Waitlist Available
Led By Ivan Pavlov, M.D.
Research Sponsored by Hôpital de Verdun
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Acute Hypercapnic respiratory failure with pH < 7.35 and pCO2 > 45 mmHg
Be older than 18 years old
Must not have
Respiratory or cardio-respiratory arrest
Hypercapnia secondary to a drug toxicity or non-pulmonary aetiology
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 hour, 6 hours, 24 hours, and daily until cessation of oxygen therapy, up to a maximum of 7 days
Awards & highlights
No Placebo-Only Group

Summary

This trial is looking at whether high flow nasal cannula (HFNC) can help people with respiratory problems who can't tolerate non-invasive ventilation (NIV).

Who is the study for?
This trial is for adults over 18 with non-severe hypercapnic respiratory failure, which means they have high levels of carbon dioxide in their blood and a lower than normal pH. It's not for those who can't read English or French, are pregnant, have certain severe conditions like shock or coma, drug-induced hypercapnia, or need immediate ventilation.
What is being tested?
The study compares two ways to give oxygen: High flow nasal cannula (HFNC) versus conventional low flow methods in patients with COPD experiencing high CO2 levels. The goal is to see if HFNC can correct gas exchange issues without needing mechanical ventilation.
What are the potential side effects?
Potential side effects may include discomfort from the nasal cannula or mask used for oxygen delivery. There could also be risks associated with receiving too much or too little oxygen such as dryness of the airways, nosebleeds, and breathlessness.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have severe breathing problems with high CO2 levels and low pH in my blood.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have not had a respiratory or heart arrest.
Select...
I have high carbon dioxide levels in my blood due to drug side effects or a non-lung related cause.
Select...
I cannot read or understand French or English.
Select...
I have high CO2 levels due to a severe asthma attack.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 hour, 6 hours, 24 hours, and daily until cessation of oxygen therapy, up to a maximum of 7 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 hour, 6 hours, 24 hours, and daily until cessation of oxygen therapy, up to a maximum of 7 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Secondary study objectives
Heart rate
Mean arterial pressure
Patient comfort
+2 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: High Flow Nasal CannulaExperimental Treatment1 Intervention
Group II: Conventional Oxygenation with low flow cannulaActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
High flow nasal cannula
2019
N/A
~930

Find a Location

Who is running the clinical trial?

Hôpital de VerdunLead Sponsor
3 Previous Clinical Trials
337 Total Patients Enrolled
Ivan Pavlov, M.D.Principal InvestigatorCIUSSS-Centre-Sud-de-l'Île-de-Montréal

Media Library

Conventional Low Flow Oxygenation (Other) Clinical Trial Eligibility Overview. Trial Name: NCT05497986 — N/A
COPD exacerbation Research Study Groups: High Flow Nasal Cannula, Conventional Oxygenation with low flow cannula
COPD exacerbation Clinical Trial 2023: Conventional Low Flow Oxygenation Highlights & Side Effects. Trial Name: NCT05497986 — N/A
Conventional Low Flow Oxygenation (Other) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05497986 — N/A
~27 spots leftby Dec 2025