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NCT07484828Not yet recruiting

Evaluation of Acid-base Disorders and Ventilation Settings in Cardiogenic Shock and Post-cardiac Arrest Patients: Comparison With VentilO Algorithm

Source: ClinicalTrials.gov · Last updated 20 Mar 2026

Brief summary (registry, in English)

This study aims to better understand how mechanical ventilation settings affect patients admitted to the coronary care unit after cardiac arrest or with cardiogenic shock. These patients often require mechanical ventilation, but current guidelines provide limited evidence on the best approach. Improper ventilation settings can lead to acid-base imbalances, such as respiratory acidosis or alkalosis, which may worsen patient outcomes. The retrospective analysis will include 100 adult patients (50 post-cardiac arrest and 50 with cardiogenic shock) who were mechanically ventilated upon admission. The study has two main objectives: Determine how often acid-base disorders occur in these patients and describe their characteristics. Compare the initial ventilator settings chosen by clinicians with those suggested by VentilO, a decision-support algorithm. The investigators will evaluate the potential effect of the VentilO recommendations on the first arterial (or capillary) blood gases compared to the real settings. This information will help refine the algorithm and guide future research on improving ventilation strategies for critically ill cardiac patients. Participation does not involve any intervention, as the study uses existing medical records.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
5 Mar 2026
Start date
May 2026
Primary completion date
Sept 2026
Lead sponsor
Laval University
NCT number
NCT07484828

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From May 2026 to the primary completion date, Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Lack of patient anthropometric data (height and weight) available in the patient record
  • No information in the record regarding the data on the humidification systems used at the time of the first blood gas test upon admission to the coronary care unit.
  • Patient stabilzed in other hospital before coronary unit admission or adjustment of respiratory parameters after a blood gas test.

Who the study is looking for

  • Adult (Age \>=18 years old)
  • Under mechanical ventilation with endotracheal tube for :
    • post cardiac arrest or cardiogenic shock
    • \- Bood gases result availability up to 4 hours after coronary unit admission

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Insitut universitaire de cardiologie et de pneumologie de Quebec - Universite Laval
Coordinator of this site? Confirm its status
QuébecCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.