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Safety Study to Evaluate the Occurrence of EFAD in Pediatric Patients With PNAC Who Require More Than Eight Weeks of Omegaven Treatment
Sponsor: Fresenius Kabi
Summary
This study will demonstrate safety in pediatric patients with Parenteral Nutrition-Associated Cholestasis treated with Omegaven®, which is indicated as a source of calories and fatty acids in this patient population
Official title: Title: A Single-arm, Open-label, Prospective, Multicenter Safety Study to Evaluate the Occurrence of Essential Fatty Acid Deficiency (EFAD) in Pediatric Patients With Parenteral Nutrition-associated Cholestasis (PNAC) Who Require More Than Eight Weeks of Omegaven Treatment
Key Details
Gender
All
Age Range
1 Day - 17 Years
Study Type
OBSERVATIONAL
Enrollment
40
Start Date
2024-12-15
Completion Date
2027-03-01
Last Updated
2025-09-05
Healthy Volunteers
No
Conditions
Interventions
Omegaven® (fish oil triglycerides) Injectable Emulsion
Pediatric patients Pediatric patients with new-onset PNAC Drug: Omegaven® (fish oil triglycerides) Injectable Emulsion Dose, frequency and duration is a decision of the Investigator
Locations (10)
Memorial Health Service
Fountain Valley, California, United States
University of California Los Angeles
Los Angeles, California, United States
The University of Chicago
Chicago, Illinois, United States
Children's Hospital Corporation d/b/a Boston Children's Hospital
Boston, Massachusetts, United States
Children's Hospital Medical Center
Cincinnati, Ohio, United States
Board of Regents of the University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States
Vanderbilt University Medical Center
Nashville, Tennessee, United States
Baylor College of Medicine Houston
Houston, Texas, United States
The University of Texas Health Science Center at San Antonio
San Antonio, Texas, United States
Seattle Children's Hospital d/b/a Seattle Children's Research Institute
Seattle, Washington, United States