Overview

Impact of Early Parenteral Nutrition Completing Enteral Nutrition in Adult Critically Ill Patients

Status:
Active, not recruiting
Trial end date:
2021-12-01
Target enrollment:
0
Participant gender:
All
Summary
In critically ill patients, a strategy aimed at an early delivery of full caloric support, with a combination of Enteral Nutrition (EN) and Parenteral Nutrition (PN) (in conditions preventing hyperglycemia and overfeeding), results in shorter ICU and hospital stay and less morbidity as compared to a strategy using only EN.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Katholieke Universiteit Leuven
KU Leuven
Collaborators:
Baxter Healthcare Corporation
Fund for Scientific Research, Flanders, Belgium
Criteria
Inclusion Criteria:

1. Patients admitted to any of the five intensive care units

2. Older than 18 years

3. Nutritional risk screening score (NRS) higher or equal to three upon ICU admission

Exclusion Criteria:

1. Patients with a do not resuscitate (DNR) code or moribund at the time of ICU admission

2. Patients already enrolled in another trial

3. Patients transferred from another intensive care unit with an established nutritional
therapy

4. Patients suffering from ketoacidotic or hyperosmolar coma on admission

5. Patients with a body mass index (BMI) below 17 kg/m^2

6. Short bowel syndrome

7. Patients known to be pregnant or nursing

8. Patients on mechanical ventilation at home

9. NRS score lower than three

10. Patient readmitted to ICU after randomization to the EPaNIC trial.

11. Patient not critically ill on admission. (No clinical indication for central
intravenous catheter or patient ready for oral nutrition on admission.)