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RECRUITING
NCT06274788

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

View on ClinicalTrials.gov

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

Interventions

DRUG

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