The goal of this worldwide observational study is to investigate ventilation practice in critically ill pediatric patients. The main questions it aims to answer are:
1. What is the global current practice of ventilatory support in critically ill pediatric patients?
2. Which potentially modifiable factors related to ventilation are associated with outcome? Participating pediatric intensive care units will gather detailed information about ventilation practice and outcome, such as duration of ventilatory support, length of ICU stay and ICU mortality.
Eligibility
Sex
ALL
Min age
—
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria:
* Expected use of (non-)invasive respiratory support for at least 12 hrs
Exclusion Criteria:
* premature infants (i.e., postconceptional age corrected for gestational age \< 40 weeks)
Primary outcome measure(s)
Tidal volume — First four days of (non-)invasive respiratory support Tidal volume
Peak inspiratory pressure — First four days of (non-)invasive respiratory support Peak inspiratory pressure
Plateau pressure — First four days of (non-)invasive respiratory support Pateau pressure
Positive end-expiratory pressure — First four days of (non-)invasive respiratory support Positive end-expiratory pressure
Driving pressure — First four days of (non-)invasive respiratory support Driving pressure
Mechanical power — First four days of (non-)invasive respiratory support Mechanical power
Trial sites (1)
Facility
City
Region
Status
UMC Groningen
Groningen
Netherlands
Recruiting
More University Medical Center Groningen trials in the Netherlands
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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