Atrial Fibrillation Clinical Trial
Official title:
Fish Oil for Atrial Fibrillation - Effect and Mechanisms
Atrial fibrillation (AF) is a heart rhythm disorder that usually involves a rapid heart rate. People who take fish oil supplements may reduce the risk of a recurrence of AF. This study will evaluate the effectiveness of fish oil at decreasing the recurrence of AF and will examine the reasons why fish oil may reduce this risk.
AF is the most common type of serious heart arrhythmia. It affects approximately 2% of the
population and is becoming more common. In AF, the heart's atria, or upper chambers,
contract in a very disorganized and abnormal manner and are unable to correctly pump blood
into the heart's ventricles, or lower chambers. Symptoms may include a rapid or irregular
pulse, dizziness, fainting, or breathing difficulty. Recent studies suggest that
inflammation plays a fundamental role in the development of AF. Inflammation, and the
resulting oxidative stress, can cause cellular and tissue damage. In turn, this may alter
heart function, potentially leading to both the onset and recurrence of AF. Markers of
inflammation, such as C-reactive protein (CRP) and interleukin-6 (IL-6), are often elevated
in patients with AF, providing further evidence of inflammation's role. While there are
several treatment options for AF, they are usually only moderately effective. Previous
research has shown that fish oil supplements have anti-inflammatory, antifibrotic, and
antioxidant effects and can reduce the risk of AF following surgery. However, it is not
known exactly how fish oil reduces this risk and whether the same positive effect will carry
over in people who experience the more common type of AF that is unrelated to surgery. The
purpose of this study is to evaluate the effectiveness of fish oil supplementation at
decreasing the recurrence of AF in adults who have not undergone recent surgery. Researchers
will also examine the ways in which fish oil reduces AF recurrence.
This study will enroll people who have had at least two occurrences of AF. Participants will
be randomly assigned to receive either fish oil supplements or placebo for 24 weeks. At
study visits at baseline and Weeks 2, 4, 8, 12, 18, and 24, participants will undergo a
medical and social history review, a physical exam, and blood and urine collection. At the
baseline study visit, an electrocardiogram will also occur.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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