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Evaluates the potential of aleglitazar to reduce cardiovascular risk in patients with a recent acute coronary syndrome (ACS) event and type 2 diabetes mellitus (T2D) Mark Bieniarz, MD Principal Investigator
ANALYZE-ST: Tests the accurary of the ST monitoring feature on Implantable Cardioverter Defibrillator (ICD). Sean Mazer, MD Principal Investigator
This study utilizes Aquapheresis Versus Intravenous Diurectics to compare these two methods of fluid removal from the heart. Robert Orchard, MD Principal Investigator
Evaluates whether the drug canakinumab reduces further events in patients who have had previous Myocardial Infarctions. Robert Orchard, MD Principal Investigator
Compares the On-X valve on low dose anticoagulation to concomitant groups of On-X valves receiving standard coumadin/aspirin therapy and to also drive FDA objective performance criteria (OPC). Paul Levy, MD Principal Investigator
Evaluates the effectiveness and safety of a Newly Devised Drug in Patients with Chronic Heart Failure. Robert Orchard, MD Principal Investigator
Pradaxa is an FDA approved blood thinning medication. Some patients who take Pradaxa develop gastrointestinal symptoms (GIS). This study evaluates the effectiveness of two kinds of treatment for GIS. Jay Tiongson, MD Principal Investigator
Compares different heart tests in identifying heart disease in patients with symptoms, and to attempt to reduce future problems with the heart. Brendan Cavanaugh, MD Principal Investigator
This study evaluates the effect of AMR101 on cardiovascular health and mortality in Hypertriglyceridemic patients with CAD or a high risk for CAD. Robert Orchard, MD Principal Investigator
Conducting risk assessment and comparative effectiveness of Left Ventricular Assist Device (LVAD) to medical management in ambulatory heart failure patients. Sean Mazer, MD Principal Investigator
The main purpose of this study is to see if Azimilide Dihydrochloride (not yet approved FDA drug) can help patients to have fewer hospitalizations/emergency department visits. Ross Downey, MD Principal Investigator
A study involving the Riata®/Riata® ST silicone endocardial leads made by St. Jude Medical. This study does not involve any investigational product (medical device) or procedures.
Post approval study of a Paclitaxel-Eluting Coronary Stent System. Robert E. Federici, MD Principal Investigator
ABSORB: A stent study for patients requiring intervention. Robert Federici, MD Principal Investigator
EVOLVE-II: To compare the safety and effectiveness of two drug-eluting stents in the treatment of coronary artery disease. Geoffrey Kunz, MD Principal Investigator
PARACHUTE IV: This Implant is intended to reduce the occurrence of death and hospitalization for heart failure by isolation of the malfunctioning portion of the left ventricle in symptomatic heart failure patients with EF<35% due to myocardial infarction in the LAD territory. Mark Bieniarz, MD Principal Investigator
SJM MultiPoint Pacing (MPP): This study is to evaluate safety and efficacy of the Quadripolar cardiac resynchronization therapy defibrillator (CRT-D) device with MultiPoint™ Pacing (MPP) feature in stimulating the left lower chamber of the heart in patients indicated for cardiac resynchronization therapy.
WARFARIN: Attempts to reduce the adverse effects of this popular blood thinner by looking at genetic variations Principal Investigator Ross Downey, MD
A prospective, randomized, open-label, parallel-group, active-controlled, multicenter study exploring the efficacy and safety of once-daily oral rivaroxaban (BAY 59-7939) compared with that of dose-adjusted oral vitamin K antagonists (VKA)for the prevention of cardiovascular events in subjects with nonvalvular atrial fibrillation scheduled for cardioversion