VentilO Prospective Study

ConditionsMechanical Ventilation Complication Respiratory Acidosis

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18+

SponsorLaval University

About this trial

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.

Eligibility criteria

Qualifiers

Adults (> 18 years old)

Intubated patients admitted to intensive care immediately post-operatively after cardiac surgery (all cardiac surgery combined)

Ventilation in controlled mode (Assist Control or SIMV)

Disqualifiers

Absence of anthropometric data (height and weight) of patients available in the patient file

Respiratory cycles mainly spontaneous on arrival

Patient extubated on arrival in intensive care

Trial design

Treatments tested in this trial

Clinicians
VenitlO

Treatment groups

76 Participants

are divided into 2 treatment groups

Sponsors and collaborators

Laval University

Lead sponsor

Source ClinicalTrials.gov