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Potential Impact of the Use of the Application VentilO After Cardiac Surgery

L

Laval University

Status

Completed

Conditions

Mechanical Ventilation Complication

Treatments

Other: VentilO application

Study type

Observational

Funder types

Other

Identifiers

NCT05886413
2023-4030

Details and patient eligibility

About

Mechanical ventilation is a vital support associated with the treatment of patients with acute respiratory failure and in other indications such as surgery under general anesthesia, coma or shock. Optimization of settings during mechanical ventilation and implementation of protective ventilation help to avoid ventilation-induced injury, ensure adequate oxygenation and maintain adequate carbon dioxide concentration to avoid respiratory acidosis or alkalosis.

Similarly, there is also no clear recommendation, to our knowledge, for the initial setting of the respiratory rate. Therefore, initial settings are not always adequate and in the literature the frequency of respiratory acidosis is very high, reaching about half of the patients receiving mechanical ventilation.

VentilO, is an application that is available on smart phones. This educational application provides clinicians with initial settings and optimization of these settings based on gender, height, weight, body temperature and patient type. The algorithm used is based on published data regarding ventilatory requirements in different populations and the anatomical and instrumental dead space of patients.

The purpose of our study is to:

Assess whether ventilatory settings after intensive care unit admission after cardiac surgery are appropriate to compare the ventilatory adjustments made by clinicians with those proposed by the VentilO application.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults (> or = 18 years old)
  • Intubated patients admitted to the ICU immediately postoperative from cardiac surgery
  • Obtained a postoperative arterial gas within 1 hour of arrival in the ICU

Exclusion criteria

  • Lack of patient anthropometric data (height and weight) available in the patient record

Trial design

100 participants in 1 patient group

Intubated patient admitted in intensive care unit at the IUCPQ-UL after cardiac surgery
Treatment:
Other: VentilO application

Trial contacts and locations

1

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Central trial contact

Pierre Alexandre Bouchard; François Lellouche

Data sourced from clinicaltrials.gov

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