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Use of Omega 3 Oil Emulsion for Parenteral Nutrition Associated Cholestasis

Clinical Trial of Omegaven™ Therapy for Parenteral Nutrition Associated Cholestasis

Status
NO_LONGER_AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT02148146
Enrollment
Unknown
Registered
2014-05-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-01-12

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

Conditions

Cholestasis

Keywords

short bowel syndrome, intestinal failure, total parenteral nutrition associated cholestasis

Brief summary

This is a clinical study designed to evaluate the safety and benefit of a fish oil based fat emulsion in the treatment of liver disease associated with prolonged use of intravenous nutrition.

Detailed description

Specific Aims of Study 1. To determine the safety profile of an intravenous omega-3 fat emulsion (Omegaven™) 2. To determine if established PN associated liver disease can be reversed or its progression halted by using a parenteral fat emulsion prepared from fish oil as measured by normalization of serum levels of hepatic enzymes and bilirubin.

Interventions

DRUGOmegaven

Fish oil emulsion given 1g/kg/day as infusion

Sponsors

University of California, San Diego
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

1. Age \< 18 years old 2. Patients will be PN dependent (unable to meet nutritional needs solely by enteral nutrition) and are expected to require PN for at least another 30 days, may be inpatient or outpatient 3. Patients considered eligible for study participation must have parenteral nutrition associated liver disease (PNALD) as defined as a direct bilirubin of 2 mg/dl or more. Other causes of liver disease should be excluded. A liver biopsy is not necessary for treatment 4. Direct bilirubin \> 2.0 mg/dl 5. Signed patient informed consent 6. The patient must have utilized standard therapies to prevent the progression of his/her liver disease including surgical treatment, cyclic PN, avoiding overfeeding, reduction/removal of copper and manganese from PN, advancement of enteral feeding, or the use of ursodiol (i.e., Actigall®)

Exclusion criteria

1. Pregnancy 2. Other causes of chronic liver disease (Hepatitis C, Cystic fibrosis, biliary atresia, and alpha 1 anti-trypsin deficiency) 3. Enrollment in any other clinical trial involving an investigational agent (unless approved by the designated physicians on the multidisciplinary team) 4. The parent or guardian or child unwilling to provide consent or assent 5. Patients known to be allergic to fish or egg protein and patients with the following contraindications to Omegaven™ use: * Impaired lipid metabolism * Severe hemorrhagic disorders * Unstable diabetes mellitus * Collapse and shock * Stroke/embolism * Recent cardiac infarction * Undefined coma status

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026