Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06826794

VentilO Prospective Study

Frequency of Respiratory Acidosis in the Intensive Care Unit After Postoperative Cardiac Surgery. Impact of Using VentilO Application

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
76 (estimated)
Sponsor
Laval University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a randomized, open-label study comparing intial settings made by clinicians with settings recommandation made by the VentilO application immediately after intensive care unit admission.The study will allow direct comparison of the frequency of acidosis when patients are ventilated using the parameters of the VentilO application versus parameters chosen by the clinician. The variables determined by the clinician or VentilO will be respiratory rate, tidal volume and resulting minute ventilation.

Conditions

Interventions

TypeNameDescription
OTHERCliniciansClinicians will determine respiratory parameters for mechanical ventilation upon arrival in the intensive care unit.
DEVICEVenitlOVentilO application (or web platerform) will determine respiratory parameters for mechanical ventilation upon arrival in the intensive care unit.

Timeline

Start date
2025-04-24
Primary completion
2026-12-01
Completion
2027-06-01
First posted
2025-02-14
Last updated
2025-09-04

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06826794. Inclusion in this directory is not an endorsement.