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
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