NCT07484828

Brief Summary

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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
5mo left

Started May 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress21%
May 2026Dec 2026

First Submitted

Initial submission to the registry

March 5, 2026

Completed
15 days until next milestone

First Posted

Study publicly available on registry

March 20, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

March 20, 2026

Status Verified

March 1, 2026

Enrollment Period

4 months

First QC Date

March 5, 2026

Last Update Submit

March 18, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Acid-base disorder (respiratory acidosis)

    Presence of respiratory acisosis define by pH\< 7.35 and PaCO2 \> 45 mmHg

    Up to 4 hours after admission to the coronary care unit - First blood gas sample

  • Acid-base disorder (respiratory alcalosis)

    Presence of respiratory alcalosis define by by pH\>7.45 and PaCO2 \< 35 mmHg

    Up to 4 hours after admission to the coronary care unit - First blood gas sample

Secondary Outcomes (10)

  • Ventilator setting (Respiratory rate)

    Up to 4 hour after coronary unit admission - At the last ventilator setting before blood gas sample

  • Ventilator setting (Tidal volume)

    Up to 4 hour after coronary unit admission - At the last ventilator setting before blood gas sample

  • Acid-base disorder (metabolic acidosis)

    Up to 4 hours after admission to the coronary care unit - First blood gas sample

  • Acid-base disorder (metabolic alcalosis)

    Up to 4 hours after admission to the coronary care unit - First blood gas sample

  • Optimal acid-base result

    Up to 4 hours after admission to the coronary care unit - First blood gas sample

  • +5 more secondary outcomes

Study Arms (2)

Patient post cardiac arrest

Other: Initiation of mechanical ventilation

Patient with cardiogenic shock

Other: Initiation of mechanical ventilation

Interventions

Blood gases evaluation after initiation of mechanical ventilation

Patient post cardiac arrestPatient with cardiogenic shock

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

post cardiac arrest or cardiogenic shock

You may qualify if:

  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Insitut universitaire de cardiologie et de pneumologie de Quebec - Universite Laval

Québec, Quebec, G1V4G5, Canada

Location

MeSH Terms

Conditions

Heart ArrestShock, Cardiogenic

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesMyocardial InfarctionMyocardial IschemiaVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosisShock

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

March 5, 2026

First Posted

March 20, 2026

Study Start

May 1, 2026

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

March 20, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations