Atrial Fibrillation
This study will compare an experimental (not yet FDA approved) blood thinner, which reduces the formation of blood clots, against Warfarin (FDA approved) in patients with Atrial Fibrillation.
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Atrial Fibrillation With Pacemakers
An experimental drug (not yet FDA approved) is being tested to see how well it works and how safe it is in eliminating episodes of atrial fibrillation in patients who have been diagnosed with Atrial Fibrillation and have a pacemaker.
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Carotid Stenting
Carotid artery stenting is necessary to hold open a carotid artery when a blockage has been diagnosed. This study is utilizing an already FDA approved device and procedure and is merely collecting additional information relative to safety and effectiveness.
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Cholesterol
The purpose of this study is to compare 2 drugs (already FDA approved) that lower LDL-C (“bad cholesterol) levels in patients who present to the hospital with chest pain.
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Congestive Heart Failure
The purpose of this study is to test if adding an experimental drug (not yet FDA approved) to your current heart failure treatment(s) is able to safely improve your heart failure.
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CRT Registry
The purpose of this registry is to evaluate the “usage patterns” of device leads and delivery systems of CRT device implantation at the time of implantation.
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Drug Eluding Stent
The purpose of this study is to compare a
newly designed drug eluding stent, (not yet FDA approved) with an already approved FDA drug eluding stent to show improved performance specific to deliverability while maintaining a similar drug release profile.
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HeartRate
The purpose of this study is to demonstrate the equivalence of experimental (not yet FDA approved) non-contact electrodes against conventional resistive contact electrodes when monitoring ECGs during the first 4 days following open-heart surgery.
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MisFit
The purpose of this study is evaluate the safety and effectiveness of an experimental drug (not yet FDA approved) in lowering the chances of having a heart attack, a stroke or dying from a heart attack or stroke in subjects with abdominal obesity at risk for such events.
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Optimization
This study will compare the capability of an already FDA approved CRT device (cardiac resynchronization therapy device) by either allowing the device to self-optimize its settings or the device will be manually programmed by the implanting doctor to optimize the settings.
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Platelet Block
The purpose of this study is to test the safety and effectiveness of an experimental drug (not yet FDA approved) that blocks platelets (platelets “stick” together and can form blood clots) when used together with standard medications for atherosclerosis.
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Valve Replacement
The purpose of this study is to define the lowest level of required antithrombotic (anti-blood clotting) therapy for prostheses in patients who have been diagnosed with heart valve disease and require replacement of their natural aortic or mitral valve.
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