Preventing Cholestasis Using SMOFLipid®

Sponsor
Medical University of Vienna (Other)
Overall Status
Completed
CT.gov ID
NCT01585935
Collaborator
(none)
230
1
2
65.4
3.5

Study Details

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.

Condition or Disease Intervention/Treatment Phase
Phase 4

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
230 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Preventing Cholestasis in Premature Infants Using SMOFLipid®
Study Start Date :
Jun 1, 2012
Actual Primary Completion Date :
Jun 1, 2015
Actual Study Completion Date :
Nov 13, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Smoflipid

SMOFLIPID will be used for parenteral lipid supply

Drug: SMOFLIPID
target dose: 3g/kg/d
Other Names:
  • SMOFLIPID (mixture of soy, fish, MCT and olive oil)
  • Active Comparator: Intralipid

    INTRALIPID will be used for parenteral lipid supply

    Drug: INTRALIPID
    target dose: 3g/kg/d
    Other Names:
  • INTRALIPID (soy bean oil)
  • Outcome Measures

    Primary Outcome Measures

    1. Incidence of parenteral nutrition associated cholestasis (PNAC) [Participants will be followed for the duration of hospital stay (expected average 14 weeks)]

      PNAC definition: Two consecutive conjugated bilirubin measurements > 1.5 mg/dl

    Secondary Outcome Measures

    1. Bailey Scales of Infant Development III [At 12 and 24 months corrected gestational age]

      Cognitive, Motor and Language Development

    Other Outcome Measures

    1. Brain maturational scores assessed by amplitude integrated EEG (aEEG) [Participants will be followed for the duration of hospital stay (expected average 14 weeks)]

      aEEG measurements of study infants performed as a part of clinical routine (as specified in the trial study protocol v 1.0-1.3)

    2. Visual Evoked Potentials (VEP) [Participants will be followed for the duration of hospital stay (expected average 14 weeks)]

      VEP measurements of study infants performed as a part of clinical routine (as specified in the trial study protocol v 1.0-1.3)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Day to 5 Days
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Medical University Vienna Vienna Austria 1090

    Sponsors and Collaborators

    • Medical University of Vienna

    Investigators

    • Study Director: Andreas Repa, MD, Medical University Vienna
    • Principal Investigator: Nadja Haiden, MD, Medical University Vienna

    Study Documents (Full-Text)

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Nadja Haiden,MD, Assoc.Prof.MD., Medical University of Vienna
    ClinicalTrials.gov Identifier:
    NCT01585935
    Other Study ID Numbers:
    • MUV-Neo2
    • 2011-005456-33
    First Posted:
    Apr 26, 2012
    Last Update Posted:
    Jan 9, 2018
    Last Verified:
    Jan 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Keywords provided by Nadja Haiden,MD, Assoc.Prof.MD., Medical University of Vienna
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 9, 2018