Trials / Completed
CompletedNCT03447457
Early Initiation of High-flow Nasal Cannula Oxygen Therapy in Patients With Acute Respiratory Failure in the Emergency Department: A Before-after Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 102 (actual)
- Sponsor
- Poitiers University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of the study is to compare the efficiency on respiratory failure regression of high-flow nasal oxygen therapy versus standard oxygen in patients admitted to the ED for de novo acute respiratory failure.
Detailed description
Prospective observational before-after study at the ED in two French centers. Selection of patients with acute hypoxemic respiratory failure at the ED. Application of oxygen strategy according to the period: * before period: standard oxygen delivered through nasal cannula, face mask or non-rebreathing reservoir mask, with a flow rate adjusted to maintain a pulse oxymetry of at least 92%. * after period: high-flow oxygen therapy continuously applied via large-bore nasal prongs with a gas flow rate of 50 L/min and a FiO2 adjusted to maintain a pulse oxymetry at least 92%.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | High-flow oxygen | HFNC is continuously applied via large-bore nasal prongs with a gas flow rate of 50 L/min and a FiO2 adjusted to maintain a pulse oxymetry at least 92% |
| DEVICE | Standard oxygen | nasal cannula, face mask or non-rebreathing reservoir mask |
Timeline
- Start date
- 2015-12-01
- Primary completion
- 2017-05-30
- Completion
- 2017-05-30
- First posted
- 2018-02-27
- Last updated
- 2018-02-27
Locations
2 sites across 1 country: France
Source: ClinicalTrials.gov record NCT03447457. Inclusion in this directory is not an endorsement.