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Effect of Supplemental Intake of Omega-3 Polyunsaturated Fatty Acids on the Rate and Complexity of Spontaneously Occurring Ventricular and Supraventricular Arrhythmias in Patients With Implantable Cardioverter Defibrillator (ICD) - A Randomized Clinical Trial

Primary Purpose

Coronary Artery Disease, Arrhythmia

Status
Unknown status
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Eicosapentanoic acid (EPA) and Docosahexanoic acid (DHA).
Sponsored by
Sheba Medical Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring CHD, Arrhythmia, ICD, Omega-3 PUFA, Nutrition

Eligibility Criteria

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

Inclusion Criteria: post-MI patients. Both single and Dual chamber ICD recipient. implanted more than 3 months ago. Agree to give written informed consent. Exclusion Criteria: Less than 18 years of age. ICD implantation as a 'bridge' to heart transplantation. Stable antiarrhythmic medication over the last month prior to enrollment. Patients taking class I antiarrhythmic medication. A projected lifespan less than one year. Participation in another trial (during or within 90 days before the study). Use of supplemental n-3 fatty acids during the last 3 months. Women who are pregnant and of childbearing potential who do not use adequate contraception. Patients known to have a history of recent drug or alcohol abuse. 10) History or current intestinal or hepatic disease.

Sites / Locations

  • The Tel Aviv Sourasky Medical Center
  • Sheba Medical Center, Heart Institute, Electrophysiology Unit

Outcomes

Primary Outcome Measures

number of VT/VF episodes

Secondary Outcome Measures

All-cause mortality, cardiac mortality, recurrent and myocardial infarction.
Atrial arrhythmia and non-sustained ventricular arrhythmia (non-sustained VT or ventricular premature complex (PVC)) as documented by ICD memory or 24 hour ECG (Holter) recording.
Whether omega-3 PUFA supplementation exerts different effects according to ischemia severity assessed by stress perfusion nuclear imaging.

Full Information

First Posted
February 9, 2006
Last Updated
November 3, 2009
Sponsor
Sheba Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT00290056
Brief Title
Effect of Supplemental Intake of Omega-3 Polyunsaturated Fatty Acids on the Rate and Complexity of Spontaneously Occurring Ventricular and Supraventricular Arrhythmias in Patients With Implantable Cardioverter Defibrillator (ICD) - A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2009
Overall Recruitment Status
Unknown status
Study Start Date
November 2005 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
June 2010 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Sheba Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
We hypothesize that oral supplementation with omega-3 PUFA will decrease occurrence of arrhythmic events among post-MI, ICD recipients.
Detailed Description
This is a randomized, placebo-controlled, crossover, double- blind interventional study. Patients will receive 3.6 g of EPA and DHA fish oil and placebo oil for 6 months, randomly, in a crossover design, with a four month washout period between treatments. Randomization will be stratified by ejection fraction (≤ 35% or > 35%), and the type of the index arrhythmia (VT - spontaneous or inducible by electrophysiologic study (EPS), versus other - VF, SCD, Primary prevention - MADIT II). Ischemia severity was chosen to be evaluated by Single Photon Emission Computed Tomography (SPECT) during stress (dipyridamol infusion). Subcutaneous adipose-tissue biopsy, a biomarker considered the gold-standard for the objective assessment of long-term habitual dietary intake of fish and marine omega-3 PUFA (EPA and DHA) will be obtain. Compliance will be monitored by counting returned capsules or bottles and by measuring the omega-3 PUFA composition in red blood cells (RBC). Three different types of questionnaires will be used in this trial to obtain more information as to the additional potential benefit of omega-3 PUFA supplementation: The newly Israeli Food Frequency Questionnaire (FFQ) will be used to examine dietary intake of other nutritional habits/patterns and its relationship to the study outcomes. The Hebrew language SF-36 health survey will be used to examine general health status. The Back questionnaires will be use to examine possible beneficial effects of fish oil supplementation on depressive symptomatology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Arrhythmia
Keywords
CHD, Arrhythmia, ICD, Omega-3 PUFA, Nutrition

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
105 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Eicosapentanoic acid (EPA) and Docosahexanoic acid (DHA).
Intervention Description
3.6 gram oral supplementation for 6 months.
Primary Outcome Measure Information:
Title
number of VT/VF episodes
Time Frame
continous
Secondary Outcome Measure Information:
Title
All-cause mortality, cardiac mortality, recurrent and myocardial infarction.
Time Frame
continous
Title
Atrial arrhythmia and non-sustained ventricular arrhythmia (non-sustained VT or ventricular premature complex (PVC)) as documented by ICD memory or 24 hour ECG (Holter) recording.
Time Frame
24 hours
Title
Whether omega-3 PUFA supplementation exerts different effects according to ischemia severity assessed by stress perfusion nuclear imaging.
Time Frame
time of the test

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: post-MI patients. Both single and Dual chamber ICD recipient. implanted more than 3 months ago. Agree to give written informed consent. Exclusion Criteria: Less than 18 years of age. ICD implantation as a 'bridge' to heart transplantation. Stable antiarrhythmic medication over the last month prior to enrollment. Patients taking class I antiarrhythmic medication. A projected lifespan less than one year. Participation in another trial (during or within 90 days before the study). Use of supplemental n-3 fatty acids during the last 3 months. Women who are pregnant and of childbearing potential who do not use adequate contraception. Patients known to have a history of recent drug or alcohol abuse. 10) History or current intestinal or hepatic disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Luria, MD
Organizational Affiliation
Sheba Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Tel Aviv Sourasky Medical Center
City
Tel Aviv
ZIP/Postal Code
64239.
Country
Israel
Facility Name
Sheba Medical Center, Heart Institute, Electrophysiology Unit
City
Tel-Hashomer
Country
Israel

12. IPD Sharing Statement

Learn more about this trial

Effect of Supplemental Intake of Omega-3 Polyunsaturated Fatty Acids on the Rate and Complexity of Spontaneously Occurring Ventricular and Supraventricular Arrhythmias in Patients With Implantable Cardioverter Defibrillator (ICD) - A Randomized Clinical Trial

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