VentilO Prospective Study
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 groupsLocations
1Institut universitaire de cardiologie et de pneumologie de Québec - Université LavalG1V4G5, QuébecQuebec, Canada
Sponsors and collaborators
Laval University
Lead sponsor
Source ClinicalTrials.gov