Effects of Omega-3 Fatty Acids on Platelets in Patients With Coronary Artery Disease With Hypertriglyceridemia (OMPA-CAD)
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| ClinicalTrials.gov Identifier: NCT01086163 |
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Recruitment Status : Unknown
Verified March 2010 by HeartDrug Research LLC.
Recruitment status was: Not yet recruiting
First Posted : March 12, 2010
Last Update Posted : March 12, 2010
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Omacor®/Lovaza® is an effective, and very safe mix of PO-3A, and the drug is currently approved by the Federal authorities for the drug management of post-infarction patients with high blood triglycerides. Given the growing length of CAD progression, it is pertinent that many more patients will yield extra benefit from Lovaza® on top of aggressive antiplatelet regimens and statin due to severity of their vascular disease. Therefore, mild antiplatelet properties of PO-3A will be a highly desirable and attractive commodity of this medication.
The investigators believe that Omacor®/Lovaza® is ideally positioned for the chronic management of CAD as a safe, efficient, and "gentle" agent with no harmful interactions with statins or aspirin.
The investigators hypothesize that addition of Omacor may add mild antiplatelet protection for CAD patients.
The study objectives are:
- To assess the ex vivo effects of Omacor® on platelet function in patients with coronary artery disease (CAD).
- To compare ex vivo platelet-related effects after 7 and 14 days of therapy with Omacor and statin combination versus statin alone in patients with chronic stable coronary heart disease.
- To establish the relation of changes in platelet activity (if any) with the lipid profile to prove an additional benefit of Omacor® on top of statin and aspirin.
| Condition or disease | Intervention/treatment |
|---|---|
| Coronary Artery Disease | Drug: Omacor, omega-3 fatty acids in CAD patients |
In terms of incidence, prevalence, morbidity, and economic costs, coronary artery disease represents a number 1 public health concern. Omacor®/Lovaza® is an effective, and very safe mix of PO-3A, and the drug is currently approved by the Federal authorities for the drug management of post-infarction patients with high blood triglycerides. Despite significant progress in the prevention and treatment of vascular disease in the Western World in the past two decades, national statistics indicate that the incidence and prevalence of heart disease has been increasing steadily. Given the growing length of CAD progression, it is pertinent that many more patients will yield extra benefit from Lovaza® on top of aggressive antiplatelet regimens and statin due to severity of their vascular disease. Therefore, mild antiplatelet properties of PO-3A will be a highly desirable and attractive commodity of this medication.
We believe that Omacor®/Lovaza® is ideally positioned for the chronic management of CAD as a safe, efficient, and "gentle" agent with no harmful interactions with statins or aspirin. Also considering low clinical incidence of aspirin-induced interactions with other classes of drugs, Lovaza® may fit nicely into a standard cocktail for diabetes, hypertension, depression, arrhythmias, and heart failure management of CAD patients, which will expand the drug utilization. However, platelet-related effects of Lovaza® on top of aspirin and statin in patients with stable coronary disease are not known, but may be important due to the high incidence of aspirin resistance and heavy burden of thrombin activation in such patients. We have a large pool of patients with documented CAD (300-350/annum), and we will be able to enroll relatively large amount of quality patients fast.
| Study Type : | Observational |
| Estimated Enrollment : | 30 participants |
| Observational Model: | Case Control |
| Time Perspective: | Prospective |
| Official Title: | Effects of Prescription OMega-3 Fatty Acids (Omacor®, Lovaza®) on Platelet Activity in Patients With Coronary Artery Disease With Hypertriglyceridemia (OMPA-CAD) |
| Study Start Date : | October 2010 |
| Estimated Primary Completion Date : | February 2011 |
| Estimated Study Completion Date : | April 2011 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Omacor dose titration
Stable documented coronary artery disease proven by angiography treated with statin and aspirin. In order to achieve homogeneity within this population, the following additional inclusion criteria will apply:
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Drug: Omacor, omega-3 fatty acids in CAD patients
Omacor 1g versus 2g daily versus placebo
Other Name: Lovaza |
- Change in platelet aggregation after Lovaza® (1 or 2g/daily) in patients treated with aspirin + simvastatin versus those matched patients treated with placebo+aspirin +simvastatin in combination. [ Time Frame: Day 7 and Day 14 ]
- Differences in expression of P-selectin and PAR-1 receptors after treatment with Lovaza® (1 or 2g/daily) in patients treated with aspirin + simvastatin versus those matched patients treated with placebo+aspirin +simvastatin in combination. [ Time Frame: Day 7 and Day 14 ]
Biospecimen Retention: Samples Without DNA
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| Ages Eligible for Study: | 50 Years to 60 Years (Adult) |
| Sexes Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- Stable documented coronary artery disease proven by angiography treated with statin and aspirin. In order to achieve homogeneity within this population, the following additional inclusion criteria will apply:
- survived first-time AMI more than 12 mths ago
- stable medical treatment during the last 3 months (except removal of Plavix)
- Ethnicity: Caucasians
- Males, 50 - 60 yrs
- Non-diabetics
- Excluded are those who eat more than one meal of fish / week
- Excluded are those who take omega-3 supplements of any sorts
Exclusion Criteria:
- Thrombolytic therapy or GP IIb/IIIa inhibitor within 30 days of enrollment
- Platelet count < 100,000
- History of bleeding disorder
- Hct < 30, serum creatinine ≥3 mg/dL, liver impairment defined as ALT/AST > 3 times upper limit of normal.
- Glomerular filtration rate <50ml/min
- Admission for acute vascular syndrome (unstable angina, MI, stroke), revascularization procedure with stent placement, or other major coronary/cerebrovascular event within 30 days.
- Active participation in other investigational drug or device trial within the last 30 days.
- Allergy or intolerance to any of the study medications.
- Antiplatelet agent other than aspirin or
- Insulin therapy
- Cancer of any localization
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01086163
| Contact: Ilya Pokov, BS | 410-371-6204 | pokov3@comcast.net | |
| Contact: Serge Surigin, BS | 443-824-2846 | serge.surigin@gmail.com |
| United States, Maryland | |
| Victor Serebruany | Recruiting |
| Towson, Maryland, United States, 21204 | |
| Contact: Ilya Pokov, BS 410-371-6204 pokov3@comcast.net | |
| Study Chair: | Alex Pokov, MD | HeartDrug Research |
| Responsible Party: | Dr. Victor Serebruany. MD, PhD, HeartDrug Research laboratories |
| ClinicalTrials.gov Identifier: | NCT01086163 History of Changes |
| Other Study ID Numbers: |
HD-Oma-09/27D |
| First Posted: | March 12, 2010 Key Record Dates |
| Last Update Posted: | March 12, 2010 |
| Last Verified: | March 2010 |
Keywords provided by HeartDrug Research LLC:
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Omacor Simvastatin Aspirin Platelet activity Coronary artery disease |
Additional relevant MeSH terms:
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Coronary Artery Disease Myocardial Ischemia Coronary Disease Hypertriglyceridemia Heart Diseases Cardiovascular Diseases Arteriosclerosis |
Arterial Occlusive Diseases Vascular Diseases Hyperlipidemias Dyslipidemias Lipid Metabolism Disorders Metabolic Diseases |