Atrial Fibrillation Clinical Trial
Official title:
A Prospective, Randomized, Double-blind Placebo-controlled Study to Determine the Efficacy of 8 mg/Day Oral Perindopril to Prevent the Recurrence of Atrial Fibrillation in Patients With Essential Hypertension
The purpose of this 7- to 13-month study is to determine the efficacy of 8 mg/day oral perindopril to prevent the recurrence of atrial fibrillation (AF) in patients with essential hypertension.
Hypertension affects approximately 50 million individuals in the United States and
approximately 1 billion individuals worldwide. As the population ages, the prevalence of
hypertension is expected to increase even further unless broad and effective preventive
measures are implemented. Recent data from the Framingham Heart Study suggest that
individuals who are normotensive at 55 years of age have a 90% lifetime risk for developing
hypertension. The relationship between blood pressure (BP) and risk of cardiovascular disease
(CVD) events is continuous, consistent, and independent of other risk factors. The higher the
BP, the greater is the chance of myocardial infarction, heart failure (HF), stroke, and
kidney disease.
Atrial fibrillation (AF) is also a major health problem and has been described as one of two
emerging cardiovascular epidemics at the turn of the century. It is the most frequent cardiac
arrhythmia, affecting 5% of individuals aged > 65 years, and it is associated with an
increased risk of stroke and a doubling of all-cause mortality. The loss of effective atrial
contraction may result in impaired cardiac performance, reduced exercise tolerance and
congestive heart failure. In addition, patients with atrial fibrillation often have disabling
palpitations.
Perindopril (Coversyl) is an angiotensin-converting enzyme (ACE) inhibitor with demonstrated
efficacy in controlling hypertension. There are several lines of evidence suggesting that ACE
inhibition may reduce the incidence of new-onset AF as well as AF recurrences.
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