Clinical Trial: Arrythmia Burden in Cardiac Contractility Modulation (CCM)
Study Status: Completed
Recruit Status: RECRUITING
Condition: Atrial Fibrillation
Study Type: OBSERVATIONAL
Official Title: Arrhythmia Burden in Patients With Impulse Dynamics Optimizer Cardiac Contractility Modulation (CCM) Device Implantation: Retrospective and Prospective Evaluation
Brief Summary:
The Impulse Dynamics Optimizer Device is a Food and Drug Administration (FDA) approved; commercially available device indicated for patients with heart failure with reduced ejection fraction (HFrEF).Many candidates of this device have a previously implanted cardiovascular implantable electronic device (CIED)- internal cardioverter defibrillator (ICD) or permanent pacemaker (PM).Patients with heart failure are at high risk for both atrial and ventricular cardiac arrhythmias.The aim of this study is to evaluate…
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