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Clinical Trials in the Netherlands / NCT01536275
Active, not recruiting Not applicable

Early Versus Late Parenteral Nutrition in the Pediatric Intensive Care Unit

NCT01536275 · tracked via the Priya Life Science Netherlands tracker
Sponsor
Phase
Not applicable
Started
2012-06
Last updated
2024-02-12

Condition(s) studied

Critical IllnessChildren

Investigational drug(s) / intervention(s)

Late parenteral nutrition

Late parenteral nutrition: Withholding parenteral nutrition during the first 7 days of ICU stay

Study summary

In the PEPaNIC trial it is investigated whether withholding parenteral nutrition during the first week in critically ill children is beneficial, compared to the current standard of the early start of parenteral nutrition.

Eligibility

Sex
ALL
Min age
—
Max age
17 Years
Healthy volunteers
No
Inclusion Criteria: * All patients admitted to the PICU with a STRONGkids score of 2 points or more upon ICU admission Exclusion Criteria: * Age of 17 years or older * Patients with a DNR code at the time of ICU admission. * Patients expected to die within 12 hours (=moribund patients). * Patient readmitted to ICU after randomization to the PEPaNIC trial, more than 48 hours after the initial discharge * Patients transferred from another paediatric intensive care after a stay of more than 7 days * Patients suffering from ketoacidotic or hyperosmolar coma on admission. * Patients suffering from Short Bowel Syndrome on home PN or other conditions that require home PN * Patients suspicious or established inborn metabolic diseases requiring specific diet * STRONGkids score lower than 2 on ICU admission. * Premature Newborns ( 37 weeks gestational age upon admission in the PICU) * Prior inclusion in another randomized controlled outcome study

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Dept Intensive Care Medicine Leuven Belgium
Stollery Children's Hospital Edmonton Alberta
Erasmus MC Sophia Kinderziekenhuis Rotterdam Netherlands

Other trials for the same condition

Official registry record

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.

View NCT01536275 on ClinicalTrials.gov ↗ ← All trials in the Netherlands