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Which Place for High Flow Oxygen in ICU ?

Which Place for High Flow Oxygen in Intensive Care Unit ?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02080208
Enrollment
20
Registered
2014-03-06
Start date
2011-02-28
Completion date
2013-06-30
Last updated
2016-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoxemia

Keywords

hypoxemia, high flow oxygen therapy, respiratory failure

Brief summary

Patients with respiratory failure often need oxygen and/or ventilatory support. Patients who need only oxygen support, usually received low flow oxygen (\< 15 Liters / min), as well as in respiratory weaning. Now new devices can be used. They provide high flow oxygen with different benefits. This high flow devices provide exact fraction of inspired oxygen (FiO2), allows a positive end expiratory pressure and supplies a wash out flow. The hypothesis of this study is that the high flow oxygen enable more efficient oxygen administration than conventional oxygen. In addition, it would improve the effectiveness of the ventilation of the patient, through flushing the dead space.

Detailed description

The investigators hypothesized that when using high flow oxygen therapy, respiratory failure is relieved, as well as ventilation failure, so accessories are less stressed muscles, and this can be demonstrated by the electromyography (EMG) of sterno-mastoid..

Interventions

DEVICEOptiflow

patients receive oxygen via high flow oxygen therapy during 20 minutes

Sponsors

Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

patients with respiratory failure. * Spontaneously breathing patient requiring administration at least 40% oxygen, or, * Patient under mechanical ventilation, during respiratory weaning.

Exclusion criteria

* Facial trauma, active hemoptysis, pneumothorax, thoraco-abdominal surgery or upcoming intubation for spontaneously breathing patients. * Neuromuscular disease, altered consciousness or agitation for patients under mechanical ventilation.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Oxygenation criteria20 minutesArterial oxygen partial pressure (PO2), oxygen saturation by pulse oximetry (SpO2), arterial PO2/FiO2, positive end expiratory pressure (PEEP)

Secondary

MeasureTime frameDescription
Change from baseline in Ventilation criteria20 minutesrespiratory rate (RR), arterial partial CO2 pressure (PCO2), pH, sterno-mastoid EMG

Other

MeasureTime frameDescription
change from baseline in hemodynamic criteria20 minutescardiac frequency, arterial blood pressure

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026