CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 22 enrolled
Drug / intervention
Intralipid 20% I.V. Fat Emulsiondrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02357576
NCT02357576Phase 3Completed

Phase 3 Study of Standard Lipid Therapy Versus Intravenous Fat Emulsion Minimization for the Prevention of Parenteral Nutrition-Associated Liver Disease

University of Michigan·interventional·Posted Feb 6, 2015·Updated Dec 17, 2020

In Brief

A Phase 3 clinical trial evaluating Intralipid 20% I.V. Fat Emulsion for Cholestasis. Completed, enrolled 22 participants across 5 sites.

Detailed Summary

Parenteral nutrition-associated cholestasis (PNAC) and liver disease (PNALD) are associated with significant morbidity and mortality in neonates and is felt to be exacerbated by soybean-based lipid emulsions. Much research is currently being directed at identifying ways to reduce this risk. Reduction of the dose of soybean-based lipid given as a component of parenteral nutrition is one possible strategy. In this study we will compare standard dosing of soybean-based lipid (up to 3/kg/day) with a minimized dose (1 g/kg/day) and evaluate for the development of cholestasis and adequate growth between the two groups. Longterm followup will include an assessment of neurodevelopmental outcomes at 12 and 24 months of age. Funding source - FDA OOPD

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCholestasis
CountriesUnited States

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedFeb 6, 2015
Enrollment StartMay 21, 2016
Primary CompletionOct 12, 2017
Study CompletionNov 8, 2019
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 11.4 years ago

Interventions

Intralipid 20% I.V. Fat Emulsiondrug