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Intravenous Nutrition in Hospitalized Patients: Comparison of Two Oils

Primary Purpose

Obstruction, Cancer, Ileus

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Intralipid
ClinOleic
Sponsored by
Johane Allard
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Obstruction focused on measuring Parenteral nutrition, lipid emulsion, Intralipid, ClinOleic, Inflammation, Infection, Bloodstream Infection, length of stay, mortality

Eligibility Criteria

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

Inclusion Criteria:

  • Patients 18 years or older

    • Patients with PN during their hospitalization
    • Patients hospitalized in medical, surgical or ICU wards
    • Signed informed consent either from the patient, their legally authorized representative or a direct family member

Exclusion Criteria:

  • • Patients without PN during their hospitalization

Sites / Locations

  • University Health Network

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Intralipid

ClinOleic

Arm Description

Patients will receive Intralipid, which is the standard lipid emulsion used in the hospital

Patients that are randomized to receive ClinOleic as a lipid emulsion in their PN, instead of Intralipid. ClinOleic is approved by Health Canada. The amount of calories from the lipid emulsion will be equivalent in the standard of care group and in the ClinOleic group.

Outcomes

Primary Outcome Measures

Prealbumin
prealbumin is an hepatic protein that is used in the diagnosis of malnutrition. It has a short half-life so any changes in nutritional status can rapidly be represented by prealbumin levels.

Secondary Outcome Measures

Length of stay
Length of stay in the hospital and ICU will be recorded. We will record how many days it took,since admission to the hospital, for the patient to be discharged. This is an expected average of 4 weeks of length of stay.
Mortality
We will follow the patients from the day of admission until the day of discharge and record the mortality, if applicable. The expected average of hospital stay is 4 weeks.
Body mass index
We will measure weight before, at day 10 and after PN to calculate the BMI at this different points. The last day of PN is whenever the patient is taken off PN. This can vary considerably from patient to patient.
Infections
we will record the infections the patients develop during PN until one week after PN
hand-grip strength
We will measure hand grip strength at baseline (day0) and at day 10 of PN. This is a test that measures the strength of the hand and forearm muscles and is often used as a general test of strength
mid-arm circumference
This is a rough indicator of body fat
Subjective global assessment (SGA)
is a bedside method that assesses the risk of malnutrition and identifies which patient will benefit best from nutrition support
Antibiotic days
we will record antibiotic days from the start of PN until one week after PN is discontinued
high sensitivity C-reactive Protein (hs-CRP)
hs-CRP is a marker of inflammation, we will measure this parameter at baseline and after 10 days of PN
Red blood cell fatty acid composition
Red blood cell fatty acid composition, particularly the essential fatty acids (linoleic acid and alpha-linolenic acid) will be measured to assess presence/absence of essential fatty acid deficiency

Full Information

First Posted
July 17, 2013
Last Updated
March 23, 2020
Sponsor
Johane Allard
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1. Study Identification

Unique Protocol Identification Number
NCT01943409
Brief Title
Intravenous Nutrition in Hospitalized Patients: Comparison of Two Oils
Official Title
Parenteral Nutrition in Hospitalized Patients: Comparison of Two Commercially Available Lipid Emulsions
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
July 2013 (Actual)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
December 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Johane Allard

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Intravenous nutrition is an important therapy for the recovery of many patients. It is indicated when the patients cannot take food by mouth or use their intestines for feeding. It is important to indicate it in the appropriate setting because it's not free of complications and is a costly treatment. Some of the complications are: elevated blood sugar or lipids, elevated liver function tests, infection of the catheter or device used to administer intravenous nutrition. Intravenous nutrition is composed by proteins, lipids, carbohydrates (sugar in the form of glucose) and vitamins. Until recently, Intralipid, a soybean oil-based lipid emulsion was the only lipid available in Canada for this kind of nutrition. Since 2010, a new lipid emulsion (ClinOleic) based on olive-oil has been approved by Health Canada for use in intravenous nutrition. There is an increasing need for hospitals to evaluate the quality of intravenous nutrition administered to hospitalized patients in terms of: assessing indications, prescription, complications, clinical results and costs. The objective of this study is to determine if intravenous nutrition prescribed in hospitalized patients is indicated following existing guidelines in terms of timing of nutrition support, prescription, monitoring and whether it is associated with complications. In addition, length of stay and mortality will be assessed. Also, we will evaluate nutritional, infectious and inflammatory parameters in patients receiving soybean oil-based lipid emulsion (Intralipid) compared to those of patients receiving olive oil-based lipid emulsion (ClinOleic).
Detailed Description
Until recently, Intralipid, a soybean oil-based lipid emulsion, has been the only available lipid for intravenous use in Canada. In 2010, ClinOleic, a new, predominantly olive oil based emulsion, has been approved by Health Canada as an alternative lipid. There is an increasing need for hospitals to do quality-assurance studies for in-patient parenteral nutrition (PN) to assess indications, PN prescription, complications, clinical outcomes and costs. The only in-patient population that is well studied is the intensive care unit (ICU) population. Several meta-analyses showed that PN was associated with higher infection rate, longer length of stay and higher mortality when compared with enteral nutrition. Results from these and other studies were the basis for the Canadian ICU Guidelines. The aim of this study is to determine if PN prescribed in in-patients is indicated, appropriately following existing guidelines in terms of timing of nutrition support, prescription and monitoring and, whether it is associated with complications. In addition, clinical outcomes such as length of stay and mortality will be assessed. Also, we will evaluate metabolic, nutritional, infectious and inflammatory parameters in patients receiving soybean oil-based lipid emulsion compared to those of patients receiving olive oil-based lipid emulsion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstruction, Cancer, Ileus, Malnutrition, Surgery
Keywords
Parenteral nutrition, lipid emulsion, Intralipid, ClinOleic, Inflammation, Infection, Bloodstream Infection, length of stay, mortality

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
303 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intralipid
Arm Type
Active Comparator
Arm Description
Patients will receive Intralipid, which is the standard lipid emulsion used in the hospital
Arm Title
ClinOleic
Arm Type
Experimental
Arm Description
Patients that are randomized to receive ClinOleic as a lipid emulsion in their PN, instead of Intralipid. ClinOleic is approved by Health Canada. The amount of calories from the lipid emulsion will be equivalent in the standard of care group and in the ClinOleic group.
Intervention Type
Drug
Intervention Name(s)
Intralipid
Intervention Description
soybean oil-based lipid emulsion
Intervention Type
Drug
Intervention Name(s)
ClinOleic
Intervention Description
olive oil-based lipid emulsion
Primary Outcome Measure Information:
Title
Prealbumin
Description
prealbumin is an hepatic protein that is used in the diagnosis of malnutrition. It has a short half-life so any changes in nutritional status can rapidly be represented by prealbumin levels.
Time Frame
at baseline (day 0) and day 10
Secondary Outcome Measure Information:
Title
Length of stay
Description
Length of stay in the hospital and ICU will be recorded. We will record how many days it took,since admission to the hospital, for the patient to be discharged. This is an expected average of 4 weeks of length of stay.
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 4 weeks
Title
Mortality
Description
We will follow the patients from the day of admission until the day of discharge and record the mortality, if applicable. The expected average of hospital stay is 4 weeks.
Time Frame
participantes will be followed for the duration of hospital stay, an expected average of 4 weeks
Title
Body mass index
Description
We will measure weight before, at day 10 and after PN to calculate the BMI at this different points. The last day of PN is whenever the patient is taken off PN. This can vary considerably from patient to patient.
Time Frame
Baseline(day 0), day 10 and last day of PN (expected after an average of 3 weeks)
Title
Infections
Description
we will record the infections the patients develop during PN until one week after PN
Time Frame
until one week post-PN (averag expected 4 weeks)
Title
hand-grip strength
Description
We will measure hand grip strength at baseline (day0) and at day 10 of PN. This is a test that measures the strength of the hand and forearm muscles and is often used as a general test of strength
Time Frame
at baseline (day 0) and day 10 of PN
Title
mid-arm circumference
Description
This is a rough indicator of body fat
Time Frame
at baseline (day0) and day 10
Title
Subjective global assessment (SGA)
Description
is a bedside method that assesses the risk of malnutrition and identifies which patient will benefit best from nutrition support
Time Frame
at baseline (day 0) and day 10
Title
Antibiotic days
Description
we will record antibiotic days from the start of PN until one week after PN is discontinued
Time Frame
until one week post PN
Title
high sensitivity C-reactive Protein (hs-CRP)
Description
hs-CRP is a marker of inflammation, we will measure this parameter at baseline and after 10 days of PN
Time Frame
Baseline (day 0) and day 10
Title
Red blood cell fatty acid composition
Description
Red blood cell fatty acid composition, particularly the essential fatty acids (linoleic acid and alpha-linolenic acid) will be measured to assess presence/absence of essential fatty acid deficiency
Time Frame
Baseline (day 0) and day 10

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients 18 years or older Patients with PN during their hospitalization Patients hospitalized in medical, surgical or ICU wards Signed informed consent either from the patient, their legally authorized representative or a direct family member Exclusion Criteria: • Patients without PN during their hospitalization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johane P Allard, MD, FRCPC
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada

12. IPD Sharing Statement

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Intravenous Nutrition in Hospitalized Patients: Comparison of Two Oils

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