Compassionate Use of Omegaven for Pediatric Patients With Parenteral Nutrition Associated Liver Disease

Sponsor
Children's Hospital of Philadelphia (Other)
Overall Status
Approved for marketing
CT.gov ID
NCT01297933
Collaborator
(none)
1

Study Details

Study Description

Brief Summary

A compassionate use protocol to provide Omegaven to pediatric patients with parenteral nutrition (PN) dependence and parenteral nutrition associated liver disease (PNALD).

Condition or Disease Intervention/Treatment Phase

Detailed Description

Omegaven is an intravenous fat emulsion (IFE) comprised of omega-3 fatty acids derived from fish oil. It will be used in an open label compassionate use treatment protocol, as an alternative to soybean oil (omega-6), as the sole IFE source of parenteral nutrition in an effort to reduce and/or reverse parenteral nutrition associated liver disease. The study will evaluate the safety and efficacy of Omegaven use in pediatric patients with PN dependence and PNALD.

Study Design

Study Type:
Expanded Access
Official Title:
Intravenous Omega-3 Fatty Acid (Omegaven) for Pediatric Patients With Total Parenteral Nutrition Associated Liver Dysfunction

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 21 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • PN dependence due to congenital or acquired gastrointestinal disease

    • Predicted PN requirement for at least an additional 30 days

    • Parenteral nutrition associated liver disease (PNALD), defined as two conjugated bilirubin levels >= 2 mg/dL at least one week apart, must be obtained to demonstrate persistence of PNALD

    • Failure to respond to standard therapies which may include cycling PN, reduction in the dose of soybean derived IFE, attempts to advance enteral feeds, ursodiol, metronidazole, and avoidance of excessive caloric provision

    • signed parent or legal guardian informed consent

    Exclusion Criteria:
    • Acute treatable infection (e.g. urinary tract infection, sepsis)

    • Known allergy to egg or fish protein

    • Contraindications to Omegaven

    • Pregnancy

    • Serum triglyceride level greater than 400 mg/dL at baseline

    • History of severe hemolytic disorders or INR greater than 1.5 at baseline (INR cutoff of greater than 2 for infants less than 1 week of age)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Children's Hospital of Philadelphia Philadelphia Pennsylvania United States 19104

    Sponsors and Collaborators

    • Children's Hospital of Philadelphia

    Investigators

    • Principal Investigator: Maria Mascarenhas, MBBS, Children's Hospital of Philadelphia

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Maria Mascarenhas, Section Chief, Clinical Nutrition, Children's Hospital of Philadelphia
    ClinicalTrials.gov Identifier:
    NCT01297933
    Other Study ID Numbers:
    • 10-007681
    First Posted:
    Feb 17, 2011
    Last Update Posted:
    Apr 12, 2019
    Last Verified:
    Apr 1, 2019
    Keywords provided by Maria Mascarenhas, Section Chief, Clinical Nutrition, Children's Hospital of Philadelphia
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 12, 2019