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Sponsored by: |
University of Dundee |
Information provided by: | University of Dundee |
ClinicalTrials.gov Identifier: | NCT00507390 |
This is a hypothesis testing study, the hypothesis being that dietary supplements of n-PUFAs concentrates are anti-arrhythmic in ventricular arrhythmic substrates.
Study Aims:To investigate whether dietary supplements of n-3 polyunsaturated fatty acid concentrates (2g PUFAs/day, Omacor) reduces MTWA (a surrogate endpoint for ventricular arrhythmia substrate) in patients with ICDs for malignant ventricular arrhythmias
Condition | Intervention | Phase |
Defibrillators, Implantable |
Dietary Supplement: n-3 polyunsaturated fatty acids (PUFAs) Dietary Supplement: olive oil |
Phase IV |
Genetics Home Reference related topics: | Brugada syndrome short QT syndrome |
MedlinePlus related topics: | Arrhythmia Dietary Supplements Pacemakers and Implantable Defibrillators |
ChemIDplus related topics: | Omacor Fish oil |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Efficacy Study |
Official Title: | The Effect of Omega-3 Polyunsaturated Fatty Acid Supplements on Microvolt T Wave Alternans in Patients With Ventricular Arrhythmia |
Estimated Enrollment: | 45 |
Study Start Date: | January 2007 |
Estimated Study Completion Date: | July 2008 |
Arms | Assigned Interventions |
A1: Active Comparator
n-3 PUFAs
|
Dietary Supplement: n-3 polyunsaturated fatty acids (PUFAs)
2g n-3 PUFAs once daily for 8 weeks
|
A2: Placebo Comparator
olive oil capsules
|
Dietary Supplement: olive oil
1 capsule day
|
Patients from the Department of Cardiology ICD out-patient clinic, Ninewells Hospital and Medical School, will be recruited. All these patients have a history of documented ventricular arrhythmia. Data from previous studies predict that 90% of these patients will have abnormal MTWA. A total of 45 ICD patients will be recruited. The study design will be a double blind randomised placebo controlled crossover design. A baseline MTWA test will be performed and patients with an abnormal test will be selected. The patients will be randomised to receive fish oil supplements (2g/day) or placebo for 8 weeks each. At the end of each intervention period, a repeat MWTA test will be performed. A 10 ml venous blood sampled will also be collected at baseline, and after each intervention period (3 samples in total). Patients in atrial fibrillation, frequent atrial or ventricular ectopics, or with ventricular pacing from the ICD, unstable angina, NYHA IV heart failure, pregnancy or child bearing potential will be excluded from the study.
End Points of the Study. The primary endpoint will be quantitative and qualitative measures of MTWA during n-3 PUFAs treatment compared to placebo.
Statistical Analysis: Quantitative differences in MTWA measurements will be analysed by a Student's t-test and qualitative differences by a chi squared test. A probability of 0.05% will be considered significant.
Ages Eligible for Study: | 21 Years to 80 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Anna Maria cHOY, MD | 44 1382 632180 | A.Choy@dundee.ac.uk |
Contact: Chim C Lang, MD | 44 1382 496375 | c.c.lang @dundee.ac.uk |
United Kingdom | |||||
Ninewells Hospital and medical School | Recruiting | ||||
Dundee, United Kingdom, DD1 9SY | |||||
Principal Investigator: Anna Maria Choy, MD |
University of Dundee |
Study Director: | Allan Struthers, MD | University of Dundee |
Study ID Numbers: | 200306ver2 |
First Received: | July 25, 2007 |
Last Updated: | July 25, 2007 |
ClinicalTrials.gov Identifier: | NCT00507390 |
Health Authority: | United Kingdom: Medicines and Healthcare Products Regulatory Agency |
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