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Stent Clinical Trials

A listing of Stent medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (212) clinical trials

A clinical study of the TAXUS® Liberté® Paclitaxel-Eluting Coronary Stent System which was previously approved by the FDA. Patient Inclusion Criteria: >years of age Patients that need a stent in the coronary arteries Patient Exclusion Criteria: Cannot receive the protocol required dual antiplatelet therapy Currently taking warfarin or similar anticoagulant ...

Phase

Humanitarian Use Device - Intracranial artery stenosis - The WingspanTM Stent System and GatewayTM PTA Balloon Catheter have been developed for the treatment of intracranial artery stenosis. Patient Inclusion Criteria: Adults > 40 years old with symptomatic stenosis of one of those intracranial arteries: Internal carotid artery (ICA ), M1 ...

Phase N/A

People with a wide-necked brain aneurysm are asked to participate in a research study being conducted by North Shore-Long Island Jewish Health System.

Phase N/A

Multi center, non-blinded, non-randomized post approval study looking at the long-term performance of the Relay Thoracic Stent Graft System with Plus Delivery System by assessing the rate of aneurysm-related mortality at 5 years post-implant.

Phase N/A

Humanitarian Use for emergent, life-threatening free perforations, aka free contrast extravasations, into the pericardium in native coronary vessels or saphenous vein bypass grafts ≥ 2.75 mm in diameter.

Phase N/A

Cardiovascular disease is the leading cause of morbidity and mortality in industrialized nations, and atherosclerosis has been linked as the chief underlying pathology. Stroke as a result of the atherosclerotic carotid artery disease (CAD) is a common cause of death and a major reason for long-term disability worldwide1. Currently, it ...

Phase N/A

The Wingspan® Stent System with Gateway® Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter was approved in the United States (US) under a Humanitarian Device Exemption (HDE) and received CE Mark in 2005. This study is being conducted to fulfill Food and Drug Administration (FDA) post market safety surveillance requirements

Phase N/A

Non-inferiority Study Comparing Firehawk Stent With Abbott Xience Family Stent (TARGET-AC)

Primary objective: to compare the MicroPort Medical (Group) Co., Ltd Firehawkcobalt chromium coronary stent ( rapamycin target eluting ) system with abluminal grooves containing a biodegradable polymer with the Abbott XIENCE family EES (Everolimus-Eluting stent) system with respect to cardiac death, myocardial infarction (not clearly attributable to a non-target vessel), ...

Phase

Sinai Vein Stent Registry

The Sinai Vein Stent Registry aims to establish and maintain a registry of patients who have undergone a vein stent placement procedure at The Mount Sinai Medical Center. The purpose of this study is to monitor and evaluate the long-term outcomes of venous stents placed to treat venous outflow obstruction. ...

Phase N/A

Harmonizing Optimal Strategy for Treatment of Coronary Artery Stenosis - Coronary Intervention With Next Generation Drug-Eluting Stent Platforms and Abbreviated Dual Antiplatelet Therapy (HOST-IDEA) Trial

Every antiplatelet-nave patient undergoing an elective procedure will be given 300 mg aspirin and loading dose of one of P2Y12 receptor inhibitors (e.g., 600 mg clopidogrel, 60 mg prasugrel or 180 mg ticagrelor) preferably 2 hours before the intervention. These loading doses can be waived for chronic antiplatelet users, and ...

Phase