About this trial

This is a multicentre prospective cohort trial in adult and pediatric ICU patients. The investigators will measure the effect of a patient's inspiratory effort during mechanical ventilation on the lungs and diaphragm. The investigators will daily (for a maximum of 8 days) measure esophageal pressures with a balloon catheter to quantify inspiratory effort and respiratory muscle function, and perform daily ultrasound measurements of the diaphragm and the lungs. The investigators hypothesize that a small inspiratory effort will result in the preservation of diaphragm function and have no adverse effect on lung function.

Eligibility criteria

Qualifiers

age > 28 days

weight > 3kg

requiring invasive mechanical ventilation

anticipated length of ventilation > 48h

Disqualifiers

refusal of consent

mechanical ventilation ≤ 2 weeks before inclusion

known anatomical malformation of the diaphragm (including congenital diaphragmatic hernia)

contra-indication to the placement of a naso-gastric esophageal balloon catheter

Trial design

Treatments tested in this trial

  • Placement of nasogastric balloon

Treatment groups

150 Participants
are divided into 1 treatment group

Locations

3
Belgium
Antwerp University Hospital (UZA)2650, EdegemAntwerp, Belgium
University Hospital Leuven (UZL)3000, Leuven Belgium
Canada
The Hospital for Sick Children (SickKids)M5G 1X8, TorontoOntario, Canada

Sponsors and collaborators

University Hospital, Antwerp

Lead sponsor

Research Foundation Flanders

Collaborator

Universitaire Ziekenhuizen KU Leuven

Collaborator

The Hospital for Sick Children

Collaborator

University of Toronto

Collaborator

Universiteit Antwerpen

Collaborator

KU Leuven

Collaborator