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

Status: Recruiting
Location: See location...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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)

Locations
Other Locations
Canada
Institut universitaire de cardiologie et de pneumologie de Québec - Université Laval
RECRUITING
Québec
Contact Information
Primary
Francois Lellouche Principal investigator, MD, PhD
francois.lellouche@criucpq.ulaval.ca
1-418-656-8711
Time Frame
Start Date: 2025-04-24
Estimated Completion Date: 2027-06
Participants
Target number of participants: 76
Treatments
Other: Clinicians
Clinicians include respiratory therapists, physcians, medical students
Active_comparator: VentilO
VentilO, smartphone application (or web plateform)
Related Therapeutic Areas
Sponsors
Leads: Laval University

This content was sourced from clinicaltrials.gov