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PREVENTING CHOLESTASIS IN PREMATURE INFANTS USING SMOFLIPID

PREVENTING CHOLESTASIS IN PREMATURE INFANTS USING SMOFLIPID - Smoflipid

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2011-005456-33-AT
Enrollment
200
Registered
2012-01-03
Start date
2012-01-26
Completion date
Unknown
Last updated
2017-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

• To compare a mixed parenteral lipid emulsion containing fish oil (SMOFlipid®) with a soybean oil based lipid emulsion (Intralipid®) for its effect on the occurrence of parenteral nutrition associated cholestasis in extremely low birth weight infants

Interventions

Trade Name: SMOFlipid 200 mg/ml Product Name: SMOFlipid 200 mg/ml Pharmaceutical Form: Emulsion for infusion Other descriptive name: OMEGA-3 FATTY ACIDS Concentration unit: mg/ml milligram(s)/millilit

Sponsors

Med. Univ. Wien, Universitätsklinik für Kinder- und Jugendheilkunde
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: • Infants born with a birth weight = 1000 Gram (= extreme low birth weight infants) • Admission to the neonatal ward in the first 24 hours of life • Informed consent obtained and randomized on study drug the first 5 days of life Are the trial subjects under 18? yes Number of subjects for this age range: 200 F.1.2 Adults (18-64 years) no F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: • Triplets or higher • Conjugated bilirubin > 1.5 mg/dl before inclusion to the study • Conditions associated with cholestasis independent of parenteral nutrition: o Inborn errors of metabolism o Viral Infections (cytomegaly virus, HIV, Hepatitis B, C) o Immune mediated hemolytic diesease (e.g. Rhesus incompatibility) o Cystic fibrosis o Primary cholestatic diseases of the liver

Design outcomes

Primary

MeasureTime frame
Main Objective: • To compare a mixed parenteral lipid emulsion containing fish oil (SMOFlipid®) with a soybean oil based lipid emulsion (Intralipid®) for its effect on the occurrence of parenteral nutrition associated cholestasis in extremely low birth weight infants ;Secondary Objective: • To assess the impact of SMOFLipid® on the long term neurocognitive development of extreme low birth weight infants at 12 and 24 months of corrected age ;Primary end point(s): ELBW infants are at high risk for development of parenteral nutrition associated cholestasis (PNAC). There is growing evidence for a positive effect of fish oil based intravenous lipid emulsions (ILE) for the treatment of PNAC. Primary use of a fish oil containing ILE for PN may prevent the development of PNAC. ;Timepoint(s) of evaluation of this end point: As long as parenteral nutrition is needed

Secondary

MeasureTime frame
Secondary end point(s): ELBW infants accumulate a deficit of ?3-LC-PUFA (especially DHA), which are important for neurodevelopment. An ILE containing fish oil provides these fatty acids and would reduce the deficit in ELBW infants, which may improve their neurocognitive development.;Timepoint(s) of evaluation of this end point: 12 to 24 month

Countries

Austria

Contacts

Public ContactDr. Repa

Med. Univ. Wien

andreas.repa@meduniwien.ac.at

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Mar 8, 2026