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Omega-3 Fatty Acids in Elderly Patients With Acute Myocardial Infarction

Giving Omega-3 Fatty Acids to Elderly Patients Diagnosed With Acute Myocardial Infarction to Investigate the Effect on Cardiovascular Morbidity and Mortality

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01841944
Acronym
OMEMI
Enrollment
1027
Registered
2013-04-29
Start date
2012-11-30
Completion date
2020-06-26
Last updated
2020-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Infarction, Heart Failure, Myocardial Revascularization, Atrial Fibrillation

Keywords

Fatty Acids, Omega-3, Aged, Myocardial Infarction

Brief summary

The aim of the present study is to investigate the possible effects of supplementation with 1.8 g/day of n-3 polyunsaturated fatty acids on cardiovascular morbidity and mortality during a follow-up period of 2 years in an elderly population after having experienced an acute myocardial infarction. The hypothesis is that this supplementation on top of modern therapy will reduce the combined cardiovascular end-point of death, non-fatal myocardial infarction, stroke, revascularizations or hospitalization for new or worsened heart failure with at least 30%.

Interventions

DRUGPikasol

Pikasol®, 3 capsules (1.8 g EPA+DHA)/day

Corn oil (56% linoleic acid, 32% oleic acid, 10% palmitic acid), unchanged and according to the manufacturer

Sponsors

University Hospital, Akershus
CollaboratorOTHER
Asker & Baerum Hospital
CollaboratorOTHER
Helse Stavanger HF
CollaboratorOTHER_GOV
Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
70 Years to 82 Years
Healthy volunteers
No

Inclusion criteria

* Patients with acute myocardial infarction discharged from hospital alive

Exclusion criteria

* Being part of another randomized trial * Documented intolerance for omega-3 fatty acids * Additional disease state that is thought to be incompatible with compliance to the study drugs * Additional disease state thought to reduce survival for the follow-up time of 2 years

Design outcomes

Primary

MeasureTime frame
Combined total mortality, first event of non-fatal myocardial infarction, stroke, revascularization or hospital admission for new or worsened heart failure.24months

Secondary

MeasureTime frame
Occurence of new onset atrial fibrillation24months

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026