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Study identifier: NCT06809309 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The Ventilation During In-hospital Cardiac Arrest Study

Condition: Cardiac Arrest (CA) · In-Hospital Cardiac Arrest · Heart Arrest  ·  Sponsor: University of Aarhus

PhaseN/A
Planned participants900
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Johannes Wittig, MD  ·  +45 78 42 00 00  ·  johannes.wittig@clin.au.dk

Kasper G Lauridsen, MD, PhD  ·  +45 78 42 00 00  ·  kglerup@clin.au.dk

Always discuss trial participation with your own doctor first.

Locations (11)

Hospital of Southern Jutland - AabenraaAabenraa, DenmarkRecruiting
Aalborg University HospitalAalborg, DenmarkRecruiting
Aarhus University HospitalAarhus, DenmarkRecruiting
Hospital of Southwest Jutland - EsbjergEsbjerg, DenmarkRecruiting
Gødstrup HospitalGødstrup, DenmarkRecruiting
North Denmark Region Hospital - HjørringHjørring, DenmarkRecruiting
Horsens Regional HospitalHorsens, DenmarkRecruiting
Odense University HospitalOdense, DenmarkRecruiting
Randers Regional HospitalRanders, DenmarkRecruiting
Viborg Regional HospitalViborg, DenmarkRecruiting
St. Olavs Hospital, Trondheim University HospitalTrondheim, NorwayRecruiting

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Source record: clinicaltrials.gov/study/NCT06809309