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NCT Number: NCT06183827

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).

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Key information

Age range

1 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre Hospitalier de la Côte Basque - Urgences, Bayonne, France

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About this study

Open-label, multicenter, prospective, cross-over cluster randomized (ratio 1:1), conducted in 16 Emergency Medical Service centers in France :

  • Experimental group: Non-Invasive Ventilation-Continuous Positive Airway Pressure (Arm 1)
  • Control group: Oxygen Supply by face mask (Arm 2)

Drowning-related acute respiratory failure has important clinical consequences (4 to 18% mortality). No national/international medical consensus exist for its management.

Our team has successively demonstrated that:

  • The acute respiratory failure related to drowning in salt or fresh water presented the same clinical pathway and prognosis ;
  • Most victims with drowning related acute respiratory failure do no present hemodynamic instability ;
  • If the oxygenation is rapidly improved, neurological status is also maintained in acute respiratory failure victims ;
  • Pediatric and adult presentations are similar.

Facing an acute respiratory failure, emergency medical service must rapidly choose between oxygen supply by face mask (15 liters /minutes), mechanical ventilation or non-invasive ventilation. mechanical ventilation as non-invasive ventilation present interests and side arms. No comparative study has been conducted between these strategies. The arguments for non-invasive ventilation use specifically in a continuous positive airway pressure mode are:

  • Fast recovery of acute respiratory failure in 24h
  • Retrospective publications showing that the benefit of non-invasive ventilation probably based on continuous positive airway pressure mode
  • Easy implementation of continuous positive airway pressure in the pre-hospital setting (adults, children, newborns)
  • Complexity of mechanical ventilation in pre-hospital setting. Our working hypothesis is the efficacy of early use of non-invasive ventilation-continuous positive airway pressure in drowning related acute respiratory failure.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 two strategies (ambivalence clause);
  • Adult Individual having signed written informed consent or child subject with an authorization of the parents.

Exclusion criteria

  • Individual with hypothermia ≤ 34°C ;
  • Individual with neurological distress defined by a Glasgow Coma Scale < 13 at first clinical assessment and during the first 15 minutes of care ;
  • Individual with hemodynamic distress defined by a systolic blood tension < 90 mmHg at first clinical assessment and during the first 15 minutes of care ;
  • Cardiac arrest or respiratory arrest ;
  • Declared pregnancy or breastfeeding ;
  • Patient under legal protection regime for adults.

Treatment and study plan

Emergency Medical Service intervention : Oxygen Supply strategy

Procedure

During the 4-month period of control, the care teams will:

  • Use Oxygen Supply by face mask (15Liters/minutes) from pre-hospital to intensive care unit admission until the 6th hour following the start of drowning care (Emergency Medical Service arrival at the scene).

Indeed, current concepts of advanced prehospital care include the use of oxygen by face mask (15Liters/minutes) and intubation-Mechanical Ventilation in case of failure. The requirement of intubation-Mechanical Ventilation by the Emergency Medical Service (pre-hospital phase) or Intensive Care Unit (hospital phase) practitioners during this first 6 hours period will be left to the discretion of the practitioners in charge of the patient;

  • Continue this strategy in the Intensive Care Unit until the Acute Respiratory Failure resolution allows a reduction of Oxygen Supply. The Oxygen Supply will be reduced progressively litter by litter each 12 hours period with maintenance of capillary saturation up to 92%.

Emergency Medical Service intervention : Continuous Positive Airway Pressure strategy

Procedure

During the 4-month period of experimentation, the care teams will:

  • Use Non-Invasive Ventilation by Continuous Positive Airway Pressure (set between 8 to 10 cm H2O) from pre-hospital setting to Intensive Care Unit admission until the 6th hour following the start of drowning care (Emergency Medical Service arrival at the scene).

The requirement of Mechanical Ventilation by the Emergency Medical Service (pre-hospital phase) or Intensive Care Unit (hospital phase) practitioners during this first 6 hours period will be left to the discretion of the practitioners in charge of the patient.

  • Continue this strategy in the Intensive Care Unit until the Acute Respiratory Failure resolution allows a reduction of Non-Invasive Ventilation-Continuous Positive Airway Pressure. Non-Invasive Ventilation-Continuous Positive Airway Pressure support will be weaned progressively (left at practitioners' convenience) with maintenance of capillary O2 saturation up to 92%.

Primary outcomes

  1. Inability to improve oxygen saturation up than 92%

    Time frame: 6 hours

    Indication of intubation/mechanical ventilation requirement in the first 6 hours based on following criteria : Inability to improve oxygen saturation up than 92% despite the ventilatory strategy used;

  2. Glasgow Coma Scale

    Time frame: 6 hours

    Indication of intubation/mechanical ventilation requirement in the first 6 hours based on following criteria : Glasgow Coma Scale < 13

  3. Cardiac arrest occurrence

    Time frame: 6 hours

    Indication of intubation/mechanical ventilation requirement in the first 6 hours based on following criteria : Cardiac arrest occurrence

  4. Systolic arterial pressure

    Time frame: 6 hours

    Indication of intubation/mechanical ventilation requirement in the first 6 hours based on following criteria : Systolic arterial pressure < 90 mmHg

  5. Aspiration

    Time frame: 6 hours

    Indication of intubation/mechanical ventilation requirement in the first 6 hours based on following criteria : Aspiration

Study contacts

Contact information is provided by the study sponsor or research team.

Pierre Michelet, MD

CONTACT

[email protected]

638741313 ext. +33

Sponsors and collaborators

Lead sponsor

Assistance Publique Hopitaux De Marseille

Other

Registry information

Official study title

Evaluation of Non-Invasive Ventilation/Continuous Positive Airway Pressure for Drowning-related Acute Respiratory Failure

Acronym: CPAPDROWNING

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Dec 28, 2023
Registry last updated
Feb 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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