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Completed

NCT Number: NCT01194063

Use of Omegaven Fish Oil Emulsion for Parenteral Nutrition Associated Liver Disease in Infants and Children

Use of a fish oil emulsion to decrease liver disease due to long term intravenous nutrition.

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Key information

Age range

Up to 18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Kapiolani Medical Center for Women and Children

Honolulu, Hawaii, 96826, United States

About this study

Unlike conventional intravenous fat emulsions, Omegaven™ is comprised solely of fish oils containing primarily omega-3 fatty acids. Animal studies have shown that IV fat emulsions such as fish oil that are high in eicosapentaenic and docosahexaenoic acids reduce impairment of bile flow as seen in cholestasis caused by conventional fat emulsions. It is thought that by administering Omegaven™ in place of conventional phytosterol/soybean fat emulsions, cholestasis may be prevented or reversed, and patients will be able to be maintained on adequate PN for growth until they are able to ingest adequate nutrition enterally. Ongoing studies are addressing safety and efficacy of Omegaven™ in the pediatric population. In this trial, infants and children with parenteral nutrition associated liver disease will receive Omegaven™ as compassionate use to potentially prevent progression of disease. Safety and efficacy are monitored.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • direct bilirubin > 2 mg/dl x2 consecutive
  • parenteral nutrition dependent, expected to continue for at least another 30 days from the first day
  • patient must have utilized standard therapies to prevent the progression of liver disease

Exclusion criteria

  • other primary cause of liver disease not parenteral nutrition-associated
  • weight <3 kg
  • infant or child enrolled in other clinical trial involving an investigational agent

Treatment and study plan

Omega-3 fish oil lipid emulsion

Drug

daily intravenous administration of Omegaven fish oil emulsion

Other names: Omegaven

Primary outcomes

  1. improving cholestasis

    Time frame: One month, 2 months, 3 months after starting omegaven and 1 month after completing treatment

    decline in serum direct bilirubin levels below 2 cm on 2 serial measures

Secondary outcomes

  1. improving liver function tests

    Time frame: 1 year

    includes ALT, AST, GGT, and triglycerides

Sponsors and collaborators

Lead sponsor

Kapiolani Medical Center For Women & Children

Other

Registry information

Official study title

Use of Omegaven for Parenteral Nutrition Associated Liver Disease

Important dates

Study start
2010
Primary completion
2018
Study completion
2019
First posted
Sep 2, 2010
Registry last updated
Apr 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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