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Observational Study of Drowning Patient's Emergency Care in Its Pre-hospital Phase.

Observational Study of Drowning Patient's Emergency Care in Its Pre-hospital Phase.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05751655
Acronym
VAR-NOYADE
Enrollment
296
Registered
2023-03-02
Start date
2023-01-18
Completion date
2023-06-13
Last updated
2026-01-26

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

Conditions

Drowning

Keywords

Drowning, Emergency medical service, Pre-hospital care, Patient outcome

Brief summary

According to the 9th edition of "NOYADES" survey, 1480 drownings accidents occurred in France in 2021, of which 146 (i.e. nearly 10%), were in the Var department. These patient's care involve in first place the Emergency Medical Service (EMS). To date, there is no recommendation from French or European academic societies of emergency medicine formalising pre-hospital care of these patients (except for the specific case of cardiac arrest). This absence of recommendation therefore favours heterogeneity of practices.

Detailed description

Within a three-year period from 2019 to 2022, this retrospective observational study aims to provide an inventory of pre-hospital practices by the EMS in the Var department and to describe drowning patients' characteristics as well as their outcome, according to the initial regulation and the type of care. These data could help for pre-hospital care management.

Interventions

OTHERPrehospital care following drowning accident

Prehospital care provided by the emergency medical service 83 (SAMU 83)

Sponsors

Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

1. Drowning patient 2. Aged 18 years old or over 3. Patient treated by pre-hospital care from the emergency medical services 83 (SAMU 83) between 1st January 2019 and 30th September 2022.

Exclusion criteria

1. Diving accident 2. Patient opposition to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Type of ventilation used in pre-hospital care3-year period from 2019-2022Mechanical ventilation, non-invasive ventilation, Continuous Positive Airway Pressure, oxygen therapy or none
Ventilatory settings used in pre-hospital care3-year period from 2019-2022Positive End Expiratory Pressure, pressure support, fraction of inspired oxygen, flow rate
Pre-hospital intervention duration3-year period from 2019-2022In minutes
Type of resources involved for pre-hospital care3-year period from 2019-2022None, fire brigade or emergency rapid response unit

Secondary

MeasureTime frameDescription
Onset of deathUp to 30 daysAnalysis according to the orientation provided by the EMS regulation (emergency rapid response unit or fire brigade) and according to the different types of care by the EMS (Oxygen therapy, non-invasive ventilation or intubation).
Duration of hospitalisationUp to 30 daysAnalysis according to the orientation provided by the EMS regulation (emergency rapid response unit or fire brigade) and according to the different types of care by the EMS (Oxygen therapy, non-invasive ventilation or intubation).
Intubation rate at hospitalUp to 30 daysAnalysis according to the orientation provided by the EMS regulation (emergency rapid response unit or fire brigade) and according to the different types of care by the EMS (Oxygen therapy, non-invasive ventilation or intubation).
Type of ventilation used at hospitalUp to 30 daysAnalysis according to the orientation provided by the EMS regulation (emergency rapid response unit or fire brigade) and according to the different types of care by the EMS (Oxygen therapy, non-invasive ventilation or intubation).

Countries

France

Contacts

STUDY_DIRECTORCélia BOUTIN, MD

Centre Hospitalier Intercommunal Toulon La Seyne sur Mer

Outcome results

None listed

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