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The Ventilation During In-hospital Cardiac Arrest Study

The Ventilation During In-Hospital Cardiac Arrest (VENT-IHCA) Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06809309
Acronym
VENT-IHCA
Enrollment
900
Registered
2025-02-05
Start date
2025-02-01
Completion date
2027-06-01
Last updated
2026-03-30

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

Conditions

Cardiac Arrest (CA), Heart Arrest, In-Hospital Cardiac Arrest

Keywords

prospective observational study, ventilation, manual ventilation, cardiac arrest, in-hospital cardiac arrest (IHCA), bag-valve-mask (BVM), tidal volume, ventilation rate, intra-arrest ventilation, cardiopulmonary ventilation (CPR), resuscitation, adult

Brief summary

The goal of this prospective observational study is to learn how ventilation quality parameters during cardiopulmonary resuscitation (CPR) are associated with short-term survival following in-hospital cardiac arrest of adult patients. 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.

Interventions

OTHERPositive 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.

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

1. In-hospital cardiac arrest 2. Age ≥ 18 years 3. \>1minute of recorded ventilation data

Exclusion criteria

1. Documented do-not-attempt cardiopulmonary resuscitation order 2. Invasive mechanical circulatory support at the time of the cardiac arrest

Design outcomes

Primary

MeasureTime frameDescription
Fraction of patients with return of spontaneous circulation (ROSC)ROSC is assessed immediately following cardiopulmonary resuscitation.ROSC is defined as sustained spontaneous circulation with no need for chest compressions for at least 20 minutes.

Secondary

MeasureTime frameDescription
Fraction of patients surviving until day 30Assessed at day 30 after cardiac arrest.Patient survival for at least 30 days following cardiac arrest.

Countries

Denmark, Norway

Contacts

CONTACTJohannes Wittig, MD
johannes.wittig@clin.au.dk+45 78 42 00 00
CONTACTKasper G Lauridsen, MD, PhD
kglerup@clin.au.dk+45 78 42 00 00
PRINCIPAL_INVESTIGATORJohannes Wittig, MD

Department of Clinical Medicine, Aarhus University, Denmark; Department of Medicine, Randers Regional Hospital, Randers, Denmark; Research Center for Emergency Medicine, Aarhus University Hospital, Denmark

PRINCIPAL_INVESTIGATORKasper G Lauridsen, MD, PhD

Department of Clinical Medicine, Aarhus University, Denmark; Department of Medicine, Randers Regional Hospital, Randers, Denmark; Research Center for Emergency Medicine, Aarhus University Hospital, Denmark;

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026