The Ventilation During In-hospital Cardiac Arrest Study
NCT ID: NCT06809309
Last Updated: 2026-01-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
900 participants
OBSERVATIONAL
2025-02-01
2027-01-31
Brief Summary
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The main questions it aims to answer are:
What ventilation volume during CPR is associated with the highest chance of return of spontaneous circulation (ROSC)? What ventilation rate during CPR is associated with the highest chance of ROSC?
Researchers will compare different levels of ventilation rates and volumes that are blindly measured during CPR to see how the observed rates and volumes are associated with survival outcomes and complications.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Study cohort
Adult patients (≥18 years) with in-hospital cardiac arrest receiving cardiopulmonary resuscitation.
Groups will be defined based on observed distribution of ventilation parameters (ventilation rate, tidal volume and minute ventilation).
Positive pressure ventilation during cardiopulmonary resuscitation
The primary exposures of interest are the observed ventilation rate, tidal volume and minute ventilation during cardiopulmonary resuscitation.
Ventilation data are obtained by inspiratory and expiratory air flow measurements using the EOlife (Archeon, Besançon, France) to which healthcare providers are blinded.
Interventions
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Positive pressure ventilation during cardiopulmonary resuscitation
The primary exposures of interest are the observed ventilation rate, tidal volume and minute ventilation during cardiopulmonary resuscitation.
Ventilation data are obtained by inspiratory and expiratory air flow measurements using the EOlife (Archeon, Besançon, France) to which healthcare providers are blinded.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Age ≥ 18 years
3. \>1minute of recorded ventilation data
Exclusion Criteria
2. Invasive mechanical circulatory support at the time of the cardiac arrest
18 Years
ALL
No
Sponsors
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University of Aarhus
OTHER
Responsible Party
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Principal Investigators
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Johannes Wittig, MD
Role: PRINCIPAL_INVESTIGATOR
Department of Clinical Medicine, Aarhus University, Denmark; Department of Medicine, Randers Regional Hospital, Randers, Denmark; Research Center for Emergency Medicine, Aarhus University Hospital, Denmark
Kasper G Lauridsen, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Department of Clinical Medicine, Aarhus University, Denmark; Department of Medicine, Randers Regional Hospital, Randers, Denmark; Research Center for Emergency Medicine, Aarhus University Hospital, Denmark;
Locations
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Hospital of Southern Jutland - Aabenraa
Aabenraa, , Denmark
Aalborg University Hospital
Aalborg, , Denmark
Aarhus University Hospital
Aarhus, , Denmark
Hospital of Southwest Jutland - Esbjerg
Esbjerg, , Denmark
Gødstrup Hospital
Gødstrup, , Denmark
North Denmark Region Hospital - Hjørring
Hjørring, , Denmark
Horsens Regional Hospital
Horsens, , Denmark
Odense University Hospital
Odense, , Denmark
Randers Regional Hospital
Randers, , Denmark
Viborg Regional Hospital
Viborg, , Denmark
St. Olavs Hospital, Trondheim University Hospital
Trondheim, , Norway
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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1-16-02-301-24
Identifier Type: REGISTRY
Identifier Source: secondary_id
2022-0367531
Identifier Type: REGISTRY
Identifier Source: secondary_id
VENT-IHCA
Identifier Type: -
Identifier Source: org_study_id
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