Clinical Trials Directory

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

TypeNameDescription
DEVICEHigh-flow oxygenHFNC 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%
DEVICEStandard oxygennasal 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.