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The main objective of this study is to evaluate the gas exchange (ventilation-perfusion ratio) with the system Optiflow® compared to facial mask among patients having an acute respiratory failure after cardiac surgery.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Optiflow | Experimental |
| |
| Facial mask | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Optiflow / Facial mask | Device | J0: randomization (Optiflow® or facial mask), lung X-ray, kinesiotherapy H0 : clinical examination, blood gas, respiratory frequency H1 : clinical examination, blood gas, respiratory frequency H6 : clinical examination, blood gas J1: clinical examination, blood gas, respiratory frequency, lung X-ray, diaphragmatic echography, kinesiotherapy J2: clinical examination, blood gas, lung X-ray, kinesiotherapy Follow-up (until withdrawal of Optiflow or facial mask): clinical examination, blood gas, lung X-ray, kinesiotherapy |
| Measure | Description | Time Frame |
|---|---|---|
| Measure of PaO2/FiO2 ratio | The main objective of this study is to evaluate the gas exchange (ventilation-perfusion ratio) with the system Optiflow® compared to facial mask among patients having an acute respiratory failure after cardiac surgery. | One hour and 24 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Scale of satisfaction completed by the patient | To evaluate the tolerance of high flow oxygen therapy: satisfaction scale | at withdrawal of oxygen system |
| Measure of pH, SatO2, PaO2, FiO2 | To evaluate hypoxia duration |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nantes University Hospital | Nantes | France |
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| ID | Term |
|---|---|
| D012131 | Respiratory Insufficiency |
| ID | Term |
|---|---|
| D012120 | Respiration Disorders |
| D012140 | Respiratory Tract Diseases |
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| 2 days |
| Number of days of hospitalization | To evaluate the duration of hospitalization with the medical device | at day 28 |
| Measure of PCO2 and respiratory frequency | To evaluate PCO2 and respiratory frequency at H+1 and J1 | One day |
| Possibility of patient transfer in conventional service | To evaluate the reception in post reanimation if transfer under oxygen therapy | at day 5 |