search
Back to results

Parenteral Lipid Emulsions and the Liver Function

Primary Purpose

Liver Failure

Status
Completed
Phase
Phase 4
Locations
Poland
Study Type
Interventional
Intervention
Lipid Emulsions, Intravenous
Sponsored by
Stanley Dudrick's Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Liver Failure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. chronic intestinal failure (CIF) receiving HPN including lipids
  2. metabolic stability on HPN for more than three months (metabolic stability = the absence of pathological laboratory resulting in the change of PN regime for at least one month)
  3. 1.0 g lipids/kg body weight per day as a part of PN

Exclusion Criteria:

  1. Existing liver failure: an elevation of SGOT, SGTP, total bilirubin, GGTP, alkaline phosphatase of more than 1.5 times x normal value
  2. Patients in whom PN was interrupted for longer than 4 continuous weeks in the preceding 6 months
  3. Patients with history of cancer and anti-cancer treatment within the last 5 years
  4. Severe hyperlipidemia
  5. Severe coagulopathy
  6. Severe renal insufficiency
  7. Acute thromboembolic events
  8. Positive test for HIV, Hepatitis B or C (from medical history)
  9. Known or suspected drug or alcohol abuse
  10. Participation in another interventional clinical trial in parallel or within three months prior to the start of this clinical trial
  11. For women with childbearing potential (i.e. females who are not chemically or surgically sterile or females who are not postmenopausal) or women of childbearing potential tested positive on standard pregnancy test (urine dipstick) or/ and lactation

Sites / Locations

  • Stanley Dudrick's Memorial Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Provision of LCT emulsions in PN

Provision of MCT/LCT emulsions in PN

Provision of Olive oil emulsions in PN

Provision of SMOF lipid emulsions in PN

Arm Description

Intervention: Lipid Emulsions, Intravenous. Daily provision of LCT-based lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.

Intervention: Lipid Emulsions, Intravenous. Daily provision of MCT/LCT lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.

Intervention: Lipid Emulsions, Intravenous. Daily provision of Olive-oil/ LCT lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.

Intervention: Lipid Emulsions, Intravenous. Daily provision of SMOF lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.

Outcomes

Primary Outcome Measures

Liver function
Measurement of bilirubin - at the beginning and every three months up to 12 months

Secondary Outcome Measures

Liver function 2
Measurement of SGTP - at the beginning and every three months up to 12 months
Liver function 3
Measurement of SGOT - at the beginning and every three months up to 12 months
Liver function 4
Measurement of GGTP - at the beginning and every three months up to 12 months
Liver function 5
Measurement of alkaline phosphatase - at the beginning and every three months up to 12 months

Full Information

First Posted
January 22, 2017
Last Updated
February 2, 2017
Sponsor
Stanley Dudrick's Memorial Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT03044639
Brief Title
Parenteral Lipid Emulsions and the Liver Function
Official Title
Four Parenteral Lipid Emulsions and the Liver Function
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
April 1, 2010 (Actual)
Primary Completion Date
October 31, 2016 (Actual)
Study Completion Date
December 31, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanley Dudrick's Memorial Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The randomized, double-blind, multi-centric study performed in four parallel groups to compare all lipid emulsions, which can be used as a part of PN. Patients with home parenteral nutrition due to stable intestinal failure, were randomly assigned to receive parenteral nutrition with one the following lipid emulsions: Long-chained triglycerides (LCT group) Medium/ long-chained triglycerides MCT/LCT (50:50, MCT/LCT group)) Olive oil/ LCT (80:20, OO group)) SMOFlipid (Omega-3/ olive oil/ MCT/ LCT, SMOF group)
Detailed Description
Intravenous lipid emulsion (IVLE) is the essential component of parenteral nutrition (PN), because it is a very efficient source of energy and essential fatty acids (FA).The prevalence of abnormal liver function tests during PN varies from 15 to 85%, according to most authors.[19-21] The severity of IFALD depends also on underlying disease, especially ongoing sepsis and pre-existing liver disease. A study comparing all lipid emulsions, which can be used as a part of PN, has never been done. The aim of the study was to compare the clinical value of the four most popular intravenous lipid emulsions in regards to the liver function in long term intestinal failure patients.Patients with home parenteral nutrition due to stable intestinal failure, were randomly assigned to receive parenteral nutrition with one the following lipid emulsions: Long-chained triglycerides (LCT group) Medium/ long-chained triglycerides MCT/LCT (50:50, MCT/LCT group)) Olive oil/ LCT (80:20, OO group)) SMOFlipid (Omega-3/ olive oil/ MCT/ LCT, SMOF group) Randomization was performed after assessment and check for in-/exclusion criteria if the patient has met all study eligibility requirements. The test emulsion became a part of regular PN admixture, which was used to feed patient at home. The study was performed for 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Failure

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized, double-blind, multi-centric study performed in four parallel groups
Masking
Investigator
Masking Description
No information on the lipid emulsion's type provided neither to the patient nor the leading physician
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Provision of LCT emulsions in PN
Arm Type
Experimental
Arm Description
Intervention: Lipid Emulsions, Intravenous. Daily provision of LCT-based lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.
Arm Title
Provision of MCT/LCT emulsions in PN
Arm Type
Experimental
Arm Description
Intervention: Lipid Emulsions, Intravenous. Daily provision of MCT/LCT lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.
Arm Title
Provision of Olive oil emulsions in PN
Arm Type
Experimental
Arm Description
Intervention: Lipid Emulsions, Intravenous. Daily provision of Olive-oil/ LCT lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.
Arm Title
Provision of SMOF lipid emulsions in PN
Arm Type
Experimental
Arm Description
Intervention: Lipid Emulsions, Intravenous. Daily provision of SMOF lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.
Intervention Type
Drug
Intervention Name(s)
Lipid Emulsions, Intravenous
Other Intervention Name(s)
parenteral lipid provision
Intervention Description
The every day provision of lipid emulsion as a part of parenteral nutrition along with dextrose, amino acids, electrolytes, trace elements, vitamins and water in the dose of 0.8-1.0 g/kg/day.
Primary Outcome Measure Information:
Title
Liver function
Description
Measurement of bilirubin - at the beginning and every three months up to 12 months
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Liver function 2
Description
Measurement of SGTP - at the beginning and every three months up to 12 months
Time Frame
12 months
Title
Liver function 3
Description
Measurement of SGOT - at the beginning and every three months up to 12 months
Time Frame
12 months
Title
Liver function 4
Description
Measurement of GGTP - at the beginning and every three months up to 12 months
Time Frame
12 months
Title
Liver function 5
Description
Measurement of alkaline phosphatase - at the beginning and every three months up to 12 months
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: chronic intestinal failure (CIF) receiving HPN including lipids metabolic stability on HPN for more than three months (metabolic stability = the absence of pathological laboratory resulting in the change of PN regime for at least one month) 1.0 g lipids/kg body weight per day as a part of PN Exclusion Criteria: Existing liver failure: an elevation of SGOT, SGTP, total bilirubin, GGTP, alkaline phosphatase of more than 1.5 times x normal value Patients in whom PN was interrupted for longer than 4 continuous weeks in the preceding 6 months Patients with history of cancer and anti-cancer treatment within the last 5 years Severe hyperlipidemia Severe coagulopathy Severe renal insufficiency Acute thromboembolic events Positive test for HIV, Hepatitis B or C (from medical history) Known or suspected drug or alcohol abuse Participation in another interventional clinical trial in parallel or within three months prior to the start of this clinical trial For women with childbearing potential (i.e. females who are not chemically or surgically sterile or females who are not postmenopausal) or women of childbearing potential tested positive on standard pregnancy test (urine dipstick) or/ and lactation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stanislaw Klek, MD PhD
Organizational Affiliation
Stanley Dudrick's Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanley Dudrick's Memorial Hospital
City
Skawina
ZIP/Postal Code
32-050
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19426581
Citation
Calder PC. Hot topics in parenteral nutrition. Rationale for using new lipid emulsions in parenteral nutrition and a review of the trials performed in adults. Proc Nutr Soc. 2009 Aug;68(3):252-60. doi: 10.1017/S0029665109001268. Epub 2009 May 11. Erratum In: Proc Nutr Soc. 2011 May;70(2):281.
Results Reference
background
PubMed Identifier
20072779
Citation
Calder PC, Jensen GL, Koletzko BV, Singer P, Wanten GJ. Lipid emulsions in parenteral nutrition of intensive care patients: current thinking and future directions. Intensive Care Med. 2010 May;36(5):735-49. doi: 10.1007/s00134-009-1744-5. Epub 2010 Jan 14.
Results Reference
background
PubMed Identifier
29960156
Citation
Klek S, Szczepanek K, Scislo L, Walewska E, Pietka M, Pisarska M, Pedziwiatr M. Intravenous lipid emulsions and liver function in adult chronic intestinal failure patients: results from a randomized clinical trial. Nutrition. 2018 Nov;55-56:45-50. doi: 10.1016/j.nut.2018.03.008. Epub 2018 Mar 22.
Results Reference
derived

Learn more about this trial

Parenteral Lipid Emulsions and the Liver Function

We'll reach out to this number within 24 hrs