Clinical Trials Logo

Clinical Trial Summary

The overall purpose of this study is to determine if replacing standard soybean oil based fat emulsions with Omegaven®, a fish oil based fat emulsion, can reverse or prevent the progression of parenteral nutrition associated liver disease. It is a compassionate use protocol for patients who already have significant liver disease related to parenteral nutrition.


Clinical Trial Description

Parenteral Nutrition (PN) is a potentially life-saving intervention for children with short bowel syndrome and intestinal failure. Many common neonatal surgical diseases including Necrotizing enterocolitis (NEC), intestinal atresias, and gastroschisis can cause intestinal failure. The recovery from these illnesses often involves prolonged periods of parenteral nutrition. Intestinal Failure Associated Liver Disease (IFALD) is the most prevalent complication of long term parenteral nutrition in children, affecting up to 2/3 of children with short bowel syndrome. Parenteral lipids are an important source of calories in children, and provide essential fatty acids. Development of IFALD is a multifactorial process. Phytosterols contained in soybean based lipid emulsions have been shown to predispose animals to IFALD. Previous studies in children have shown that dosing the soybean based parenteral lipid emulsion at doses greater than 1g/kg/day may contribute to the development of IFALD. It is currently our practice to limit the lipid dose in children at risk of development of IFALD to 1g/kg/day. Despite this, some patients will still develop biochemical evidence of cholestasis and IFALD. Previous studies in humans have shown that children with IFALD who were administered the intravenous fish oil lipid emulsion Omegaven® reduced their serum direct bilirubin levels. This may be due to a reduction in the amount of arachidonic acide derived inflammatory mediators. The investigators hypothesize that administering Omegaven® in place of conventional soybean fat emulsions may reverse or prevent the progression of PN associated cholestasis and thus allow the patient to be maintained on adequate PN until he/she is able to ingest adequate nutrition enterally. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02328768
Study type Expanded Access
Source University of Nebraska
Contact
Status Approved for marketing
Phase

See also
  Status Clinical Trial Phase
Completed NCT02370251 - Compassionate Use of Omegaven in Children Phase 2/Phase 3
Completed NCT01845116 - Omegaven® in the Treatment of Parenteral Nutrition (PN) Induced Liver Injury Phase 2
Withdrawn NCT01323907 - Compassionate Use of Omegaven IV Fat Emulsion N/A
Recruiting NCT01565278 - Fish Oil for Patients With Liver Disease Due to Parenteral Nutrition Phase 3
Terminated NCT00816348 - Compassionate Use of Omegaven IV Fat Emulsion Phase 2
Completed NCT02534077 - Intravenous Fat Emulsion Comprised of Fish Oil in the Treatment of Parenteral Nutrition Induced Liver Injury in Infants Phase 3
Approved for marketing NCT01412359 - Compassionate Use of Omegaven® in the Treatment of Parenteral Nutrition Associated Hepatic Injury
Approved for marketing NCT02929303 - Expanded Access of Omegaven IV Fat Emulsion to Infants and Children With PNALD
Approved for marketing NCT02780193 - Intravenous Fish Oils in the Treatment of Parenteral Nutrition Liver Injury