Drowning-related Acute Respiratory Failure
The purpose of this study is to assess the Non-Invasive Ventilation-Continuous Positive Airway Pressure efficacy (experimental group) for drowning related Acute Respiratory Failure compared to Oxygen Supply by face mask (15Liters/minutes) (control group).
| Condition(s) | Drowning |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | The purpose of this study is to assess the Non-Invasive Ventilation-Continuous Positive Airway Pressure efficacy (experimental group) for drowning related Acute Respiratory Failure compared to Oxygen Supply by face mask (15Liters/minutes) (control group). |
| Who can participate | Inclusion Criteria: * Man/boy or woman/girl, 1yo and older. * Subject suffering from drowning related-Acute Respiratory Failure (whatever the nature of water, salt or fresh) and benefiting from the Emergency Medical Service intervention; * Acute Respiratory Failure defined as the presence of: * Capillary O2 saturation \<92% upon Emergency Medical Service first clinical analysis at the drowning scene; * Need for oxygen supply 15Liters/minutes to reach capillary O2 saturation ≥ 95%; * Combination of Acute Respiratory Failure clinical signs: at least 1 of the following items: respiratory rate \>30/min, sternal or clavicular indrawing, abdominal breathing, cyanosis. * Individual affiliated to or beneficiary of a French health insurance system; * Individual with the ability to benefit from the |
| Ages | 1 Year |
| Sex | All |
| Lead sponsor | Assistance Publique Hopitaux De Marseille |
| Locations | Bayonne, France; Bordeaux, France; La Rochelle, France; Les Sables-d'Olonne, France; Marseille, France; Montpellier, France (+3 more sites) |
| Start date | 2024-07-24 |
| NCT ID | NCT06183827 |
| Official listing | https://clinicaltrials.gov/study/NCT06183827 |