Parenteral Nutrition Associated Liver Disease Clinical Trial
Official title:
Olive Oil and Soybean 1 Oil Based Intravenous Lipid Emulsions, Liver Biochemistry and Clinical Outcomes
Background: Intravenous lipid emulsions (IVLE) are an essential component of parenteral
nutrition (PN). Omega-6 reducing strategies may improve outcomes, including reduced PN
associated liver disease.
Objective: The primary objective was to compare serum alkaline phosphatase (ALP), among
surgical and medical patients provided with either Intralipid or Clinoleic lipid emulsions.
Design: In this quasi-experimental study the medical records of surgical and medical adult
patients were reviewed from 3 Canadian hospitals that received PN with either soybean oil
(Intralipid) or predominantly olive oil (Clinoleic) based lipid emulsions for at least 7
consecutive days.
A few small studies have shown that a predominantly olive oil based IVLE is well tolerated
and safe, however the clinical relevance of this IVLE is uncertain as no clear benefit in
outcomes has been observed in small randomized clinical trials. Given the limited data
available for the adult population reporting on the experience with olive oil based IVLE, we
designed a quasi-experimental study to review our experience with Clinoleic compared to
Intralipid. The primary objective was to compare the impact of Intralipid and Clinoleic IVLE
on serum alkaline phosphatase (ALP), pre-PN to after one week of PN (i.e. between day 8 to 16
post-PN initiation), while controlling for the ordered lipid dosing. Secondary objectives
were to assess if there were differences between the IVLEs on the remaining liver function
tests, lipid dosing, incidence of infectious complications, length of stay in hospital and
30- day mortality.
This retrospective quasi-experimental chart review was conducted in 3 tertiary care hospitals
in Calgary, AB between July 01, 2012 to June 30, 2013 and July 01, 2014 to June 30, 2015.
Standard soybean oil-based therapy, Intralipid was the only available IVLE in Calgary, AB
until July 2013, at which time predominantly olive oil Clinoleic was approved as an
alternative in the hospital formulary, accounting for the dates chosen for the study. Ethics
approval from the Conjoint Health Research and Ethics Board at the University of Calgary was
obtained prior to the initiation of the study.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00910104 -
Cholestasis Reversal: Efficacy of IV Fish Oil
|
Phase 2/Phase 3 | |
Recruiting |
NCT01157780 -
Parenteral Nutrition Associated Liver Disease: Early Markers and Therapy Wih Enteral Omega-3 Supplementation
|
N/A | |
Completed |
NCT00862446 -
Use of Omega-3 Fat Emulsion (Omegaven) in Infants With Parenteral Nutrition Associated Liver Disease
|
Phase 4 | |
Completed |
NCT05181085 -
Study of NST-6179 in Healthy Subjects
|
Phase 1 | |
Completed |
NCT02010034 -
Compassionate Use of Omegaven in the Treatment of Parenteral Nutrition Induced Hepatic Injury
|
N/A | |
Completed |
NCT05347888 -
How Well do we Feed the Critically Ill Patients
|
||
Withdrawn |
NCT04807478 -
Safety of Omegaven in Pediatric Patients With Parenteral Nutrition-Associated Cholestasis (PNAC)
|
||
No longer available |
NCT02121769 -
Omegaven Expanded Access Protocol
|
||
Approved for marketing |
NCT03561194 -
Omegaven Protocol:Intermediate Size Patient Population
|