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Early Versus Late Parenteral Nutrition in the Pediatric Intensive Care Unit (PEPaNIC)

Primary Purpose

Critical Illness, Children

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Late parenteral nutrition
Sponsored by
KU Leuven
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Illness focused on measuring critical illness, children, nutrition, metabolism

Eligibility Criteria

undefined - 17 Years (Child)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Dept Intensive Care MedicineRecruiting
  • Stollery Children's Hospital
  • Erasmus MC Sophia KinderziekenhuisRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Early parenteral nutrition

Late parenteral nutrition

Arm Description

Parenteral nutrition supplements insufficient enteral nutrition from admission to ICU according to the current standard of care per center

Parenteral nutrition will be withheld during the first 7 days of ICU stay

Outcomes

Primary Outcome Measures

Incidence of new infection during ICU stay
Duration of ICU dependency (crude stay days and time to alive discharge from ICU)

Secondary Outcome Measures

Mortality
Time to alive discharge from hospital
Incidence of hypoglycaemia during ICU stay
Time to final weaning from mechanical respiratory support
Incidence of liver dysfunction during ICU stay
Need for haemodynamic support during ICU stay
Incidence of new kidney injury during ICU stay
Duration of antibiotics treatment during ICU stay
Number of readmissions to the ICU
Amount of calories delivered during the ICU stay and in subset markers of feeding intolerance
Markers of inflammation such as C-reactive protein concentrations during ICU stay
Structural and or functional differences in muscle tissue during ICU stay
biochemical, metabolic, endocrine, immunological, inflammatory and (epi)genetic markers on blood samples
with healthy matched control group
functional and neurocognitive development
with healthy matched control group
health economy analysis
total health care costs during hospital stay

Full Information

First Posted
February 16, 2012
Last Updated
March 8, 2022
Sponsor
KU Leuven
Collaborators
Sophia Kindergeneeskunde, Stollery Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01536275
Brief Title
Early Versus Late Parenteral Nutrition in the Pediatric Intensive Care Unit
Acronym
PEPaNIC
Official Title
Impact of Early Parenteral Nutrition Completing Enteral Nutrition in Paediatric Critically Ill Patients
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 2012 (undefined)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
KU Leuven
Collaborators
Sophia Kindergeneeskunde, Stollery Children's Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness, Children
Keywords
critical illness, children, nutrition, metabolism

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
1440 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Early parenteral nutrition
Arm Type
No Intervention
Arm Description
Parenteral nutrition supplements insufficient enteral nutrition from admission to ICU according to the current standard of care per center
Arm Title
Late parenteral nutrition
Arm Type
Experimental
Arm Description
Parenteral nutrition will be withheld during the first 7 days of ICU stay
Intervention Type
Other
Intervention Name(s)
Late parenteral nutrition
Other Intervention Name(s)
Late PN
Intervention Description
Withholding parenteral nutrition during the first 7 days of ICU stay
Primary Outcome Measure Information:
Title
Incidence of new infection during ICU stay
Time Frame
during ICU stay and up to 90 days post-randomization
Title
Duration of ICU dependency (crude stay days and time to alive discharge from ICU)
Time Frame
during ICU stay and up to 90 days post-randomization
Secondary Outcome Measure Information:
Title
Mortality
Time Frame
during ICU stay, hospital stay and up to 90 days post-randomization
Title
Time to alive discharge from hospital
Time Frame
during hospital stay and up to 90 days post-randomization
Title
Incidence of hypoglycaemia during ICU stay
Time Frame
during the intervention window up to day 8 post-randomization
Title
Time to final weaning from mechanical respiratory support
Time Frame
during ICU stay and up to 90 days post-randomization
Title
Incidence of liver dysfunction during ICU stay
Time Frame
during ICU stay and up 90 days post-randomization
Title
Need for haemodynamic support during ICU stay
Time Frame
during ICU stay and up 90 days post-randomization
Title
Incidence of new kidney injury during ICU stay
Time Frame
during ICU stay and up 90 days post-randomization
Title
Duration of antibiotics treatment during ICU stay
Time Frame
during ICU stay and up to 90 days post-randomization
Title
Number of readmissions to the ICU
Time Frame
up to 90 days post-randomization
Title
Amount of calories delivered during the ICU stay and in subset markers of feeding intolerance
Time Frame
during the intervention window of 8 days and up to 90 days post-randomization
Title
Markers of inflammation such as C-reactive protein concentrations during ICU stay
Time Frame
during ICU stay and up to 90 days post-randomization
Title
Structural and or functional differences in muscle tissue during ICU stay
Time Frame
during ICU stay and up to 90 days post-randomization
Title
biochemical, metabolic, endocrine, immunological, inflammatory and (epi)genetic markers on blood samples
Description
with healthy matched control group
Time Frame
up to 4 years post-randomization
Title
functional and neurocognitive development
Description
with healthy matched control group
Time Frame
up to 4 years post-randomization
Title
health economy analysis
Description
total health care costs during hospital stay
Time Frame
during index hospitalization

10. Eligibility

Sex
All
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tom Fivez, MD
Phone
003216340989
Email
tom.fivez@uzleuven.be
First Name & Middle Initial & Last Name or Official Title & Degree
Dieter Mesotten, MD PhD
Phone
003216340977
Email
dieter.mesotten@med.kuleuven.be
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Greet Van den Berghe, MD PhD
Organizational Affiliation
KU Leuven
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept Intensive Care Medicine
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tom Fivez, MD
Phone
003216340989
Email
tom.fivez@uzleuven.be
First Name & Middle Initial & Last Name & Degree
Dieter Mesotten, MD PhD
Phone
003216340977
Email
dieter.mesotten@med.kuleuven.be
First Name & Middle Initial & Last Name & Degree
Dieter Mesotten, MD PhD
First Name & Middle Initial & Last Name & Degree
Tom Fivez, MD
Facility Name
Stollery Children's Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2B7
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Erasmus MC Sophia Kinderziekenhuis
City
Rotterdam
ZIP/Postal Code
3015
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sascha Verbruggen, MD, PhD
Phone
0031107036669
Email
s.verbruggen@erasmusmc.nl
First Name & Middle Initial & Last Name & Degree
Koen Joosten, MD, PhD
Phone
0031107040704
Email
k.joosten@erasmusmc.nl

12. IPD Sharing Statement

Citations:
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Citation
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PubMed Identifier
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Citation
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Results Reference
derived
PubMed Identifier
35549984
Citation
Vanhorebeek I, Jacobs A, Mebis L, Dulfer K, Eveleens R, Van Cleemput H, Wouters PJ, Verlinden I, Joosten K, Verbruggen S, Van den Berghe G. Impact of critical illness and withholding of early parenteral nutrition in the pediatric intensive care unit on long-term physical performance of children: a 4-year follow-up of the PEPaNIC randomized controlled trial. Crit Care. 2022 May 12;26(1):133. doi: 10.1186/s13054-022-04010-3.
Results Reference
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PubMed Identifier
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Citation
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Results Reference
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Citation
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Results Reference
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Citation
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Citation
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Early Versus Late Parenteral Nutrition in the Pediatric Intensive Care Unit

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