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Oxepa in Multiple Trauma (OMT)

Primary Purpose

Multiple Trauma, Head Trauma

Status
Unknown status
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Oxepa (enteral nutrition formula, ABBOTT), at a dose determined by a patient's energy expenditure and tolerance of enteral feeding.
oxepa
Control group
Sponsored by
Rabin Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Trauma focused on measuring Mechanical Ventilation

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Males and females aged 18-90 years with multiple-trauma or head trauma admitted to the ICU.
  2. Enteral nutrition can be initiated within 36 hours of admission/ injury.
  3. Mechanical ventilation.

Exclusion criteria:

  1. Severe underlying systemic disease and /or treatment with immunosuppressive agents.
  2. Contra-indication for Enteral Nutrition (mechanical or functional bowel. obstruction, high-output fistula, severe necrotizing pancreatitis).
  3. 2nd /3rd degree burns covering > 66% BSA.
  4. Pregnancy.
  5. Participants under the age of 18.

Sites / Locations

  • Rabin Medical Center, Campus BeilinsonRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Oxepa

Control group

Arm Description

Oxepa (enteral nutrition formula, ABBOTT)will be administered at a dose determined by a patient's energy expenditure and tolerance of enteral feeding.

Pulmocare or Jevity (enteral nutrition formula, ABBOTT)will be administered at a dose determined by a patient's energy expenditure and tolerance of enteral feeding.

Outcomes

Primary Outcome Measures

Oxygenation (PO2/FIO2 ratio)
PO2/FIO2 ratio; assessed by measuring arterial blood gases (AVL Omni Technology, Graz, Austria) and ventilator settings (10)

Secondary Outcome Measures

TNF-α, CRP (markers of inflammatory response)
Concentration of circulating inflammatory markers: TNF-α, CRP concentrations
Fatty acid composition of RBC phospholipids, including n-3:n-6 ratio (markers of n-3 PUFA incorporation into blood cell membranes)
Fatty acid composition of RBC membrane (thin liquid chromatography)

Full Information

First Posted
April 1, 2010
Last Updated
November 21, 2013
Sponsor
Rabin Medical Center
Collaborators
Israeli Ministry of Security
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1. Study Identification

Unique Protocol Identification Number
NCT01099501
Brief Title
Oxepa in Multiple Trauma
Acronym
OMT
Official Title
Oxepa in Multiple Trauma: Prospective, Randomized, Comparative, Double-blind, Controlled Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Unknown status
Study Start Date
April 2010 (undefined)
Primary Completion Date
May 2014 (Anticipated)
Study Completion Date
August 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rabin Medical Center
Collaborators
Israeli Ministry of Security

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a single-center, prospective, randomized, comparative, double-blind controlled clinical study mend to assess the effect of enteral feeding with Oxepa (a fish oil-based nutrition), compared to an isocaloric control, on oxygenation and clinical outcomes in mechanically ventilated trauma patients. The study population will be adults admitted to the ICU due to multiple-trauma or head trauma as a result of a gun shut, motor vehicle accidents, fall, workplace accident etc.
Detailed Description
Primary outcome: Improvement in oxygenation Secondary outcomes: Significant improvement in other clinical and laboratory end points. Primary endpoint: Pulmonary function: Oxygenation (PO2- FIO2 ratio) Incidence of ALI Length of Ventilation (LOV) Secondary endpoints: Rate of complications: -New organ failure. Rate of new infections: -wound infection, bacteremia, ventilation associated pneumonia. Pain: -Pain score and analgesic use Morbidity/ mortality: Length of ICU stay Length of hospitalization 28 day mortality Hospital mortality All patients will commence enteral feeding via a nasogastric or orogastric tube; allocation to either Oxepa or Pulmocare/Jevity (control group) will be determined by randomization code. Patients will be prescribed to receive a daily amount of enteral formula that provides at least 80% of their energy; the latter will be calculated every 48 to 72 hours by Indirect Calorimetric (IC) measurement of Resting Energy Expenditure (REE). Tolerance of EN will be assessed by measurement of Gastric Residual Volume (GRV) every 8 hrs and the mode of feeding will be modified accordingly. Treatment: Enrolled patients will be randomly divided into a control group and an intervention group. Control group treatment: Will be administered Pulmocare or Jevity (enteral nutrition formula, ABBOTT), at a dose determined by a patient's energy expenditure and tolerance of enteral feeding. Intervention group treatment: Will be administered with Oxepa (enteral nutrition formula, ABBOTT), at a dose determined by a patient's energy expenditure and tolerance of enteral feeding. Treatment duration: The above formulas will be/delivered until the first of the following occurs: patients resume regular oral feeding day 28/ discharge from ICU/ exitus Patients transferred to Total Parenteral Nutrition Note: the attending physician according to the patient's needs will determine feeding of patients from there on. Study termination (end of all study procedures): day 28/ discharge from ICU Patients transferred to Total Parenteral Nutrition before day 3 of the study

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Trauma, Head Trauma
Keywords
Mechanical Ventilation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Oxepa
Arm Type
Active Comparator
Arm Description
Oxepa (enteral nutrition formula, ABBOTT)will be administered at a dose determined by a patient's energy expenditure and tolerance of enteral feeding.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Pulmocare or Jevity (enteral nutrition formula, ABBOTT)will be administered at a dose determined by a patient's energy expenditure and tolerance of enteral feeding.
Intervention Type
Dietary Supplement
Intervention Name(s)
Oxepa (enteral nutrition formula, ABBOTT), at a dose determined by a patient's energy expenditure and tolerance of enteral feeding.
Intervention Description
Oxepa will be administered(enteral nutrition formula, ABBOTT), at a dose determined by a patient's energy expenditure and tolerance of enteral feeding
Intervention Type
Dietary Supplement
Intervention Name(s)
oxepa
Intervention Description
A dose determined by a patient's energy expenditure and tolerance of enteral feeding.
Intervention Type
Dietary Supplement
Intervention Name(s)
Control group
Intervention Description
Pulmocare or Jevity (enteral nutrition formula, ABBOTT)will be administered at a dose determined by a patient's energy expenditure and tolerance of enteral feeding.
Primary Outcome Measure Information:
Title
Oxygenation (PO2/FIO2 ratio)
Description
PO2/FIO2 ratio; assessed by measuring arterial blood gases (AVL Omni Technology, Graz, Austria) and ventilator settings (10)
Time Frame
2 years
Secondary Outcome Measure Information:
Title
TNF-α, CRP (markers of inflammatory response)
Description
Concentration of circulating inflammatory markers: TNF-α, CRP concentrations
Time Frame
2 years
Title
Fatty acid composition of RBC phospholipids, including n-3:n-6 ratio (markers of n-3 PUFA incorporation into blood cell membranes)
Description
Fatty acid composition of RBC membrane (thin liquid chromatography)
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females aged 18-90 years with multiple-trauma or head trauma admitted to the ICU. Enteral nutrition can be initiated within 36 hours of admission/ injury. Mechanical ventilation. Exclusion criteria: Severe underlying systemic disease and /or treatment with immunosuppressive agents. Contra-indication for Enteral Nutrition (mechanical or functional bowel. obstruction, high-output fistula, severe necrotizing pancreatitis). 2nd /3rd degree burns covering > 66% BSA. Pregnancy. Participants under the age of 18.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pierre Singer, Principal Investigator MD
Phone
972-3-9376521
Email
psinger@clalit.org.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pierre Singer, MD, Professor
Organizational Affiliation
Rabin Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rabin Medical Center, Campus Beilinson
City
Petach Tikva
ZIP/Postal Code
49100
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre Singer, MD
Phone
972-39376521
Email
psinger@clalit.org.il
First Name & Middle Initial & Last Name & Degree
Milana Grinev, Study Coordinator
Phone
972-39376521
Email
milang@clalit.org.il
First Name & Middle Initial & Last Name & Degree
Shaul Lev, MD
First Name & Middle Initial & Last Name & Degree
Ilya Kagan, MD
First Name & Middle Initial & Last Name & Degree
Miriam Ben Harosh Katz, MD
First Name & Middle Initial & Last Name & Degree
Milana Grinev, RN
First Name & Middle Initial & Last Name & Degree
Miriam Theilla, RN, MSC
First Name & Middle Initial & Last Name & Degree
Shapiro Haim, MD
First Name & Middle Initial & Last Name & Degree
Ronit Anbar, RD
First Name & Middle Initial & Last Name & Degree
Dana Pinsker, RD

12. IPD Sharing Statement

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Oxepa in Multiple Trauma

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