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Ventilation in Cardiac Arrest Resuscitation Study

An Evaluation of Manual Ventilation Practices of Professional Firefighters During Cardiopulmonary Resuscitation.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05992454
Acronym
VECARS
Enrollment
120
Registered
2023-08-15
Start date
2023-05-26
Completion date
2024-02-01
Last updated
2024-02-22

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

Conditions

Basic Cardiac Life Support, CardioPulmonary Resuscitation, Heart Arrest, Out-Of-Hospital

Keywords

heart arrest, cardiopulmonary resuscitation, bag-valve-mask, rescuers

Brief summary

Out-of-hospital cardiac arrest (OHCA) is a major public health problem, with around 40,000 victims each year in France. Their survival rate remains dramatically low, at less than 10%. In the event of pre-hospital cardiac arrest, rescuers perform resuscitation techniques using equipment for which they have been trained. They perform cardiopulmonary resuscitation (CPR) by alternating 30 chest compressions with 2 insufflations (30/2) with a manual insufflator bag. In basic life supports, insufflations should result in chest rise, but guidelines do not specify a precise volume. Recently, medical devices have been developed that enable precise measurement of ventilatory volumes. In simulation, these devices show hyperventilation in volume and frequency in mannequins. But no clinical study has analyzed insufflator bag ventilation maneuvers in real-life situations on pre-hospital cardiac arrest patients. The aim of this study is to analyze ventilation parameters in current practice in relation to standards, and the factors influencing the quality of ventilation maneuvers.

Interventions

DEVICEEOLIFE

Measurement of ventilatory parameters during manual ventilation by professional rescuers during out-of-hospital cardiac arrest

Sponsors

Fire Brigade Of Paris Emergency Medicine Dept
CollaboratorOTHER
French Defence Health Service
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Out of hospital cardiac arrest with CPR performed by the Firefighters * Age 18 and over * BLS team on site before arrival of physician staffed ALS means * CPR ventilation initially provided with Bag-valve- mask * Measuring device records ventilatory parameters

Exclusion criteria

* trauma related OHCA * airway obstruction during CPR * OHCA on hanging * tracheostomized patient * obstacle to using the Bag-valve-mask * CPR time less than 2 minutes

Design outcomes

Primary

MeasureTime frameDescription
Tidal volumeup to 20 minutes (end of BLS-CPR)Measurement of volume (mL) provided by the BLS Teams \[air + oxygen\] for each manual insufflation performed by the rescuer

Secondary

MeasureTime frameDescription
Ventilation rateup to 20 minutes (end of BLS-CPR)Ventilation rate per min. achieved by the rescuer
Insufflation timeup to 20 minutes (end of BLS-CPR)Insufflation time (seconds) per ventilation procedure
chest riseup to 20 minutes (end of BLS-CPR)concomitant chest rise (YES/NO) during each ventilation procedure
Volume received by the patientup to 20 minutes (end of BLS-CPR)Volume received (mL) by the patient per ventilation procedure
Survival to day 60 after cardiac arrestup to 60 daysSurvival curve over the first 60 days
Face mask leakageup to 20 minutes (end of BLS-CPR)face mask leakage per ventilation procedure

Countries

France

Outcome results

None listed

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