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CAvent-Ventilation During Advanced Cardiopulmonary Resuscitation in Out-of-hospital Cardiac Arrest- an Observational Study

NCT04237727 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 241

Last updated 2026-04-07

No results posted yet for this study

Summary

The aim of this observational study is to investigate how ventilations is given during cardiopulmonary resuscitation (CPR) given by advanced life support providers (ALS). A portable device capable of detailed measurments of ventilation will be used when ventilating patients suffering cardiac arrest.

The main objective of the study is to describe the ventilatiosn given in terms of volume, frequency and pressure, both overall and during different CPR modes and when using different methods to handle the patients airway.

Conditions

  • Out-of-Hospital Cardiac Arrest
  • Pulmonary Ventilation

Interventions

DEVICE

Fluxmed GrH portable pneumotachograph

Fluxmed GrH portable pneumotachograph is used to measure the given ventilation. It is placed on the chosen airway adjunct and passively measures ventilation parameters such as volumes, and flow.

Sponsors & Collaborators

  • Regionale Ambulance Voorziening, Amersfoort, Utrecht, Netherlands

    collaborator UNKNOWN

  • Amsterdam UMC

    collaborator OTHER

  • Dalarna County Hospital, Falun, Sweden

    collaborator UNKNOWN

  • Capio AB Rapid Response Cars, Stockholm, Sweden

    collaborator UNKNOWN

  • Uppsala University

    lead OTHER

Principal Investigators

  • Sten Rubertsson, PhD · Uppsala University department of surgical sciences

  • David Smekal, PhD · Uppsala University department of surgical sciences

  • Johan Mällberg, BsSC · Uppsala University department of surgical sciences

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-01
Primary Completion
2025-08-31
Completion
2025-12-01

Countries

  • Netherlands
  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04237727 on ClinicalTrials.gov