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OpenTrials
Completed

NCT Number: NCT03662282

Omegaven as Alternative Parenteral Fat Nutrition

To provide Omegaven® as a compassionate treatment for critically ill infants with parenteral nutrition associated cholestasis

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Key information

Age range

14 day and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

USF Health

Tampa, Florida, 33606, United States

About this study

An intermediate population, Investigational New Drug study, to provide an alternate intravenous fat nutrition, Omegaven®, to help improve liver function while providing adequate nutrition for critically ill infants with parenteral nutrition associated cholestasis

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Greater than 14 days old
  • Has parenteral nutrition associated cholestasis defined as at least 2 consecutive direct bilirubin >2 mg/dL with anatomical or functional short gut (OR >4 mg/dL if intact intestine) obtained at least 1 week apart with a ratio of direct: total bilirubin > 0.4
  • Patient is parenteral nutrition dependent (unable to meet nutritional needs solely by enteral nutrition) and are expected to require parenteral nutrition for at least 3 more weeks
  • Patient has not responded to other therapeutic approaches for parenteral nutrition-associated liver disease such as : cycling of parenteral nutrition, avoiding overfeeding, reduction/removal of copper and manganese from parenteral nutrition, advancement of enteral feeding, and use of Ursodiol
  • Patient has been on at least 2 weeks of SMOFLIPIDs with no improvement or worsening of direct bilirubin levels
  • Signed patient informed consent
  • The patient is expected to have a reasonable possibility of survival
  • No other known etiology of cholestasis other than parenteral nutrition-associated liver disease at the time of Omegaven® initiation

Exclusion criteria

  • Known causes of cholestasis other than parenteral nutrition-associated liver disease including but not limited to Hepatitis C, Cystic fibrosis, biliary atresia, and alpha 1 antitrypsin deficiency are present, prior to Omegaven® initiation
  • Known fish or egg allergy
  • Any of the contraindications to use of Omegaven®:
  • Active new infection at the time of initiation of Omegaven®
  • Hemodynamic instability
  • Recent use of medications with associated risk of bleeding, including NSAIDs
  • Active coagulopathy or bleeding
  • Platelet counts persistently under 30,000 despite transfusions
  • Unstable hyperglycemia
  • Impaired lipid metabolism (triglycerides >1000 mg/dL) while on 1 g/kg/day or less of Intralipid
  • History of severe hemorrhagic disorders (ie. hemophilia, Von Willebrand disease, etc.)
  • Unstable diabetes mellitus
  • Collapse and shock
  • Stroke/ Embolism
  • Cardiac infarction within the last 3 months
  • Undefined coma status

Treatment and study plan

Omegaven

Drug

Omegaven® fat emulsion will be used as a compassionate use treatment for critically ill infants with parenteral nutrition associated liver injury

Primary outcomes

  1. Number of Participant With Decrease in Direct Bilirubin Level

    Time frame: First month of treatment

    Number of participant with decrease in direct bilirubin levels within 30 days of treatment

Secondary outcomes

  1. Number of Participant With Resolution of Direct Hyperbilirubinemia

    Time frame: 2 months

    Number of participant with Direct bilirubin level of <2mg/dL at discontinuation of treatment

  2. Number of Participant With Preservation of Length

    Time frame: Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment

    Monitoring of weekly length while the patient is receiving Omegaven® treatment

  3. Number of Participant With Preservation of Head Circumference

    Time frame: Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment

    Monitoring of weekly head circumference while the patient is receiving Omegaven® treatment

  4. Number of Participant With Preservation of Normal Weight Gain

    Time frame: Weekly measurement during treatment. Evaluation every 30 days from treatment initiation until discontinuation of treatment, patient hospital discharge, whichever comes first, or up to 6 months following initiation of treatment

    Monitoring of daily weight gain while the patient is on Omegaven®

Sponsors and collaborators

Lead sponsor

University of South Florida

Other

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Sep 7, 2018
Registry last updated
Jul 22, 2020

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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