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Preventing Cholestasis Using SMOFLipid®

Primary Purpose

Cholestasis, Psychomotor Disorders, Developmental

Status
Completed
Phase
Phase 4
Locations
Austria
Study Type
Interventional
Intervention
SMOFLIPID
INTRALIPID
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cholestasis focused on measuring Infant, Extremely Low Birth Weight, Parenteral Nutrition, Fish Oils, Cholestasis, Psychomotor Disorders, Developmental

Eligibility Criteria

1 Day - 5 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Birth weight ≤ 1000 Gram
  • Admission to the neonatal ward in the first 24 hours of life
  • Informed consent and randomization in the first 5 days of life

Exclusion Criteria:

  • Triplets or higher
  • Conjugated bilirubin > 1.5 mg/dl before inclusion to the study
  • Conditions associated with cholestasis independent of parenteral nutrition, i.e. inborn errors of metabolism, viral infections (cytomegaly virus, HIV, Hep B, Hep C), immune mediated hemolytic disease (Rhesus incompatibility), cystic fibrosis and any other primary cholestatic disease
  • Congenital neurological malformations for secondary outcome

Sites / Locations

  • Medical University Vienna

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Smoflipid

Intralipid

Arm Description

SMOFLIPID will be used for parenteral lipid supply

INTRALIPID will be used for parenteral lipid supply

Outcomes

Primary Outcome Measures

Incidence of parenteral nutrition associated cholestasis (PNAC)
PNAC definition: Two consecutive conjugated bilirubin measurements > 1.5 mg/dl

Secondary Outcome Measures

Bailey Scales of Infant Development III
Cognitive, Motor and Language Development

Full Information

First Posted
April 16, 2012
Last Updated
January 6, 2018
Sponsor
Medical University of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT01585935
Brief Title
Preventing Cholestasis Using SMOFLipid®
Official Title
Preventing Cholestasis in Premature Infants Using SMOFLipid®
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
June 2012 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
November 13, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Vienna

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Preterm infants of extreme low birth weight (ELBW, < 1000 gram birth weight) cannot immediately be nourished with mother´s or formula milk and are typically dependent on parenteral nutrition (PN) for a prolonged period of time. This puts them at risk for liver complications of PN, namely parenteral nutrition associated cholestasis (PNAC). Intravenous lipid emulsions (ILE) based on soy bean oil are standard of care for provision of energy and essential fatty acids in preterm infants. However, they might be implicated in the pathogenesis of PNAC. ILEs based on pure fish oil are proposed for therapy of PNAC. Recently a lipid emulsion containing 15 % fish oil together with soy bean, olive and MCT oil has become available in Europe (SMOFLIPID®). Such a balanced lipid emulsion might be more favourable than the standard soy bean oil emulsion (Intralipid®) concerning the development of PNAC. Furthermore ILEs containing fish oil might exert a positive effect on neurodevelopment. However, there are no data so far. The study aims to evaluate the fish oil containing ILE "SMOFlipid®" for its protective effect against PNAC in ELBW infants compared to standard treatment with the soy bean based ILE "Intralipid®". Furthermore neurodevelopment at 12 and 24 months of corrected gestational age will be investigated.
Detailed Description
BACKGROUND: Extreme low birth weight infants (ELBW, < 1000 gram birth weight) are typically dependent on parenteral nutrition (PN) for a prolonged period of time. This puts them at risk for development of liver complications of PN, namely parenteral nutrition associated cholestasis (PNAC). Intravenous lipid emulsion (ILE) based on soy bean oil are standard of care in preterm infants, but might be implicated in the pathogenesis of PNAC. Fish oil is rich in omega-3 long chain polyunsaturated fatty acids (LC-PUFA) that particularly accumulate in liver and brain of the fetus during the last trimester of pregnancy. In pediatric patients, ILEs based on pure fish oil are proposed as a rescue therapy of PNAC. Recently a mixed lipid emulsion containing 15 % fish oil together with soy bean , olive and MCT oil has become available for PN in Europe. Such a balanced lipid emulsion might be more favourable than the standard soy bean oil emulsion (Intralipid®) concerning the development of PNAC. Furthermore ILEs containing fish oil might exert a positive effect on neurodevelopment. However there are no data so far. AIM: To evaluate a fish oil containing ILE (SMOFlipid®) for its prophylactic effect on PNAC in ELBW infants compared to a soy bean based ILE (Intralipid®). STUDY DESIGN: Double blind prospective randomized trial. Primary Outcome: PNAC defined as two conjugated bilirubin > 1.5 mg/dl measurements on two consecutive occasions. Secondary Outcome: The most important secondary outcome is neurodevelopment at 12 and 24 months of corrected age. Exploratory Outcomes: Brain maturation measured by amplitude integrated EEG (aEEG) and flashed visual evoked potentials as available from clinical routine examinations HYPOTHESIS: The use of a mixed lipid emulsion containing fish oil (SMOFLIPID®) will reduce the incidence of PNAC compared to a standard soy bean oil based lipid emulsion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholestasis, Psychomotor Disorders, Developmental
Keywords
Infant, Extremely Low Birth Weight, Parenteral Nutrition, Fish Oils, Cholestasis, Psychomotor Disorders, Developmental

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
230 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Smoflipid
Arm Type
Experimental
Arm Description
SMOFLIPID will be used for parenteral lipid supply
Arm Title
Intralipid
Arm Type
Active Comparator
Arm Description
INTRALIPID will be used for parenteral lipid supply
Intervention Type
Drug
Intervention Name(s)
SMOFLIPID
Other Intervention Name(s)
SMOFLIPID (mixture of soy, fish, MCT and olive oil)
Intervention Description
target dose: 3g/kg/d
Intervention Type
Drug
Intervention Name(s)
INTRALIPID
Other Intervention Name(s)
INTRALIPID (soy bean oil)
Intervention Description
target dose: 3g/kg/d
Primary Outcome Measure Information:
Title
Incidence of parenteral nutrition associated cholestasis (PNAC)
Description
PNAC definition: Two consecutive conjugated bilirubin measurements > 1.5 mg/dl
Time Frame
Participants will be followed for the duration of hospital stay (expected average 14 weeks)
Secondary Outcome Measure Information:
Title
Bailey Scales of Infant Development III
Description
Cognitive, Motor and Language Development
Time Frame
At 12 and 24 months corrected gestational age
Other Pre-specified Outcome Measures:
Title
Brain maturational scores assessed by amplitude integrated EEG (aEEG)
Description
aEEG measurements of study infants performed as a part of clinical routine (as specified in the trial study protocol v 1.0-1.3)
Time Frame
Participants will be followed for the duration of hospital stay (expected average 14 weeks)
Title
Visual Evoked Potentials (VEP)
Description
VEP measurements of study infants performed as a part of clinical routine (as specified in the trial study protocol v 1.0-1.3)
Time Frame
Participants will be followed for the duration of hospital stay (expected average 14 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
5 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Birth weight ≤ 1000 Gram Admission to the neonatal ward in the first 24 hours of life Informed consent and randomization in the first 5 days of life Exclusion Criteria: Triplets or higher Conjugated bilirubin > 1.5 mg/dl before inclusion to the study Conditions associated with cholestasis independent of parenteral nutrition, i.e. inborn errors of metabolism, viral infections (cytomegaly virus, HIV, Hep B, Hep C), immune mediated hemolytic disease (Rhesus incompatibility), cystic fibrosis and any other primary cholestatic disease Congenital neurological malformations for secondary outcome
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreas Repa, MD
Organizational Affiliation
Medical University Vienna
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Nadja Haiden, MD
Organizational Affiliation
Medical University Vienna
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After publication of the trial, we currently plan to share IPD upon personal request.
IPD Sharing Time Frame
After publication for 10 years.
IPD Sharing Access Criteria
We are planning to publish the protocols together with the statistical analysis plan as supplemental information. This however depends on the respective journal. Otherwise please request the study protocol together with the statistical analysis plan from the study director andreas.repa@meduniwien.ac.at
Citations:
PubMed Identifier
32590001
Citation
Thanhaeuser M, Fuiko R, Oberleitner-Leeb C, Brandstaetter S, Binder C, Thajer A, Huber-Dangl M, Haiden N, Pablik E, Berger A, Repa A. A Randomized Trial of Parenteral Nutrition Using a Mixed Lipid Emulsion Containing Fish Oil in Infants of Extremely Low Birth Weight: Neurodevelopmental Outcome at 12 and 24 Months Corrected Age, A Secondary Outcome Analysis. J Pediatr. 2020 Nov;226:142-148.e5. doi: 10.1016/j.jpeds.2020.06.056. Epub 2020 Jun 23.
Results Reference
derived
PubMed Identifier
31030946
Citation
Binder C, Giordano V, Thanhaeuser M, Kreissl A, Huber-Dangl M, Longford N, Haiden N, Berger A, Repa A, Klebermass-Schrehof K. A Mixed Lipid Emulsion Containing Fish Oil and Its Effect on Electrophysiological Brain Maturation in Infants of Extremely Low Birth Weight: A Secondary Analysis of a Randomized Clinical Trial. J Pediatr. 2019 Aug;211:46-53.e2. doi: 10.1016/j.jpeds.2019.03.039. Epub 2019 Apr 25.
Results Reference
derived
PubMed Identifier
29269199
Citation
Repa A, Binder C, Thanhaeuser M, Kreissl A, Pablik E, Huber-Dangl M, Berger A, Haiden N. A Mixed Lipid Emulsion for Prevention of Parenteral Nutrition Associated Cholestasis in Extremely Low Birth Weight Infants: A Randomized Clinical Trial. J Pediatr. 2018 Mar;194:87-93.e1. doi: 10.1016/j.jpeds.2017.11.012. Epub 2017 Dec 18.
Results Reference
derived
Links:
URL
http://www.fwf.ac.at/en/about-the-fwf/corporate-policy/
Description
Homepage of the Austrian Science Fund (FWF)
URL
http://www.meduniwien.ac.at/homepage/service/vienna-general-hospital-akh/en/
Description
Vienna General Hospital, Medical University of Vienna

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Preventing Cholestasis Using SMOFLipid®

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