Trials / Completed
CompletedNCT03443479
Comparison of High-flow Oxygen vs. BiPAP in Type II (Hypercapnic) Respiratory Failure
Retrospective Cohort Study of Patients With Type II (Hypercapnic) Respiratory Failure Treated With High-flow Oxygen Therapy Versus Non-invasive Ventilation With BiPAP
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 324 (actual)
- Sponsor
- Hôpital de Verdun · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A retrospective cohort study of all patients treated for type II (hypercapnic) respiratory failure with either High-Flow Oxygen Therapy or Non-Invasive Ventilation in a general adult hospital.
Detailed description
We will compare various clinically relevant outcomes in patients treated for type II (hypercapnic) acute respiratory failure (ARF) with either High-Flow Nasal Cannula (HFNC) or Non-Invasive Ventilation (NIV) in a general adult hospital. All patients treated with HFNC were treated with an Optiflow device (Fisher\&Paykel). Various Bilevel positive airway pressure (BiPAP) devices were used during the study period. All ventilatory parameters were set according to the treating physicians' preferences.
Conditions
- Respiratory Failure
- Respiratory Insufficiency
- Respiratory Tract Diseases
- COPD
- COPD Exacerbation
- Pneumonia
- Chronic Obstructive Pulmonary Disease
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Non-Invasive Ventilation | Treatment with Non-Invasive Ventilation by BiPAP. Different BiPAP models are in use. Ventilation parameters set at the discretion of the treating physician. |
| DEVICE | High-Flow Nasal Cannula | Treatment with a High-Flow Nasal Cannula. The Optiflow device by Fisher\&Paykel used in all cases. Flow and fraction of inspired oxygen (FiO2) parameters at the discretion of the treating physician. |
Timeline
- Start date
- 2015-04-01
- Primary completion
- 2019-07-01
- Completion
- 2019-07-01
- First posted
- 2018-02-23
- Last updated
- 2020-07-28
Locations
1 site across 1 country: Canada
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03443479. Inclusion in this directory is not an endorsement.