Irbesartan for the Prevention of Atrial Arrhythmias and Cardiac Electrical Remodeling in Patients With Hypertension and Permanent Pacemakers
Atrial Fibrillation, Hypertension
About this trial
This is an interventional prevention trial for Atrial Fibrillation focused on measuring Atrial Fibrillation, Arrhythmia, Pacemaker, Artificial, Atrial High Rate Episodes, Electrophysiology, Renin-Angiotensin System, Hypertension, Cardiac Remodeling
Eligibility Criteria
Inclusion Criteria: Sinus Node Dysfunction (with or without AV conduction disturbance) Permanent, atrial or dual-chamber pacemaker implanted > 2 months before enrollment and with ability to record and store atrial high-rate episodes, frequency of mode switches and to perform non-invasive electrophysiologic testing History of at least 6 AHRE in the last 6 months (rate > 220/min, duration of > 2 minutes History of prior diagnosis of hypertension and/or treated for hypertension OR two documented BP > 130/85 (measurements done at least one week apart) Exclusion Criteria: Permanent or persistent AF or more than 6 episodes of symptomatic paroxysmal AF in the previous 6 months Documented Cr >200 umol/L and K+ >5.2 mmol/L in the previous 3 months Current treatment with a potassium sparing diuretic, unless serum potassium known to be in the normal range LV ejection fraction known to be < 40 % Moderate or severe mitral regurgitation (3+, 4 +) Mitral stenosis of more than mild severity Aortic stenosis with mean gradient of > 25 mmHg Angina at rest in the last 2 months, or current CCS Class 3 or 4 angina Unipolar atrial lead Previous AV node ablation P-wave amplitude less than 1.5 mV Current therapy with an ACE inhibitor, ARB or aldosterone antagonist Current or planned (within 6 months) with an anti-arrhythmic medication (amiodarone, sotalol, flecainide, propafenone, quinidine, dofetilide
Sites / Locations
- Population Health Research Institute of McMaster University