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Clinical trial

A Randomized, Double-Blind, Controlled, Clinical Trial to Evaluate the Risk of Developing Essential Fatty Acid Deficiency in Pediatric Patients, Including Neonates, Receiving Either Clinolipid (Lipid Injectable Emulsion, USP) 20% or Standard-of-Care Soybean Oil-Based Lipid Emulsion (Part A)

NCT04555044 is registered in ClinicalTrials.gov with Baxter Healthcare Corporation as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Double-Blind, Controlled, Clinical Trial to Evaluate the Risk of Developing Essential Fatty Acid Deficiency in Pediatric Patients, Including Neonates, Receiving Either Clinolipid (Lipid Injectable Emulsion, USP) 20% or Standard-of-Care Soybean Oil-Based Lipid Emulsion (Part A)
Lead sponsor
Baxter Healthcare Corporation
Phase
Phase 4
Overall status
Completed
Start date
January 22, 2021
Completion date
November 16, 2022
Enrollment
101 (actual)
Sites
9

Conditions

As the registry lists them; a condition with its own page is linked.

essential fatty acid deficiency (efad)