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Carotid Artery Diseases clinical trials

View clinical trials related to Carotid Artery Diseases.

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NCT ID: NCT01343667 Completed - Clinical trials for Cardiovascular Diseases

GORE Flow Reversal System and GORE Embolic Filter Extension Study

FREEDOM
Start date: April 2011
Phase: N/A
Study type: Interventional

The objective of this study is to provide an ongoing evaluation of clinical outcomes associated with the GORE Flow Reversal System and the GORE Embolic Filter when used for embolic protection during carotid artery stenting.

NCT ID: NCT01264419 Completed - Clinical trials for Carotid Artery Diseases

Silk Road Medical First in Man Study - Neuroprotection During Carotid Stenting and Angioplasty

PROOF
Start date: March 2009
Phase: N/A
Study type: Interventional

Cerebral embolization during carotid artery stenting (CAS) can often precipitate severe adverse neurological effects. Most major clinical studies of CAS have used distal filters for cerebral protection and have compared the neurologic complication rates with those of carotid endarterectomy (CEA). Many currently available embolic protection devices, however, have limited efficacy in capturing microembolic debris that is liberated during stenting, pre-dilatation and post-dilatation. Distal protection systems are furthermore limited by the need to cross the lesion prior to deployment. Some studies have shown a relatively high incidence of cerebral infarction even when distal protection devices are employed. Cerebral protection with carotid flow reversal is a method that was developed by Parodi, et al., as an alternative to the use of distal protection devices. While novel in its approach, this method too has its limitations. Criado, et al., developed a derivative technique that employs carotid flow reversal prior to traversing the stenosis and can be accomplished by directly accessing carotid anatomy without the use of the transfemoral approach. Major benefits to this method include the ability to perform the procedure on patients with severe carotid tortuosity and difficult aortic arch anatomy.

NCT ID: NCT01203982 Completed - Clinical trials for ST-segment Elevation Myocardial Infarction

Effect of Intensive Lipid Lowering Treatment Compared to Moderate Lipid Lowering Treatment on Carotid Intima-media Thickness (CIMT)

Start date: November 2007
Phase: Phase 4
Study type: Interventional

The aim of this study was to measure the effect of moderate and intensive lipid-lowering treatment with rosuvastatin on the carotid intima-media thickness (CIMT) as a surrogate marker of cardiovascular risk.

NCT ID: NCT01178320 Completed - Clinical trials for Coronary Artery Disease

Carotid Plaque Characteristics by MRI in AIM-HIGH (Carotid MRI Substudy)

Start date: March 2008
Phase: N/A
Study type: Observational

Heart attacks and strokes caused by the unstable atherosclerotic plaques remain the leading cause of death in the United States. Unstable plaques often have more fat than stable plaques. This study will investigate if a treatment with LDL-lowering plus HDL-raising compared with LDL-lowering alone would more effectively reduce the plaque fat content assessed by magnetic resonance imaging (MRI), therefore, further reducing heart attacks and strokes.

NCT ID: NCT01133327 Completed - Stroke Clinical Trials

Adapt Monorail Carotid Stent System: A Postmarket Clinical Follow-up Study

ASTI
Start date: June 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to get outcomes data for the Adapt Monorail Carotid System used in conjunction with the FilterWire Embolic protection system for treatment of patients that suffer from carotid artery stenosis and that cannot have surgery due to high risk factors.

NCT ID: NCT00812383 Completed - Clinical trials for Carotid Artery Disease

Carotid With Bivalirudin Angioplasty

COBRA
Start date: August 2003
Phase: Phase 2
Study type: Interventional

Single center randomized clinical trial, to evaluate the safety and efficacy of carotid artery stenting using the RX ACCULINKâ„¢ Carotid Stent System with RX ACCUNETâ„¢ Embolic Protection System or PercuSurge GuardWire® 3-6 Temporary Occlusion and Aspiration System using Angiomax (bivalirudin)versus heparin as the anticoagulant for treatment of occlusive carotid artery disease in low and high risk patient cohorts.

NCT ID: NCT00804843 Completed - Clinical trials for Carotid Atherosclerosis

Merck Carotid Atherosclerosis Trial (MK-0000-111)(COMPLETED)

MCAT
Start date: April 2009
Phase: Phase 2
Study type: Interventional

This study will examine the effect of statin and niacin therapy on carotid plaque biomarkers

NCT ID: NCT00798512 Completed - Clinical trials for Carotid Artery Disease

Diffusion Weighted-MRI Based Evaluation of the Effectiveness of Endovascular Clamping During Carotid Artery Stenting With the Mo.Ma Device.

DESERVE
Start date: February 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to detect new ischemic lesions after carotid artery stenting (with the Cristallo Ideale stent), in patients with high grade carotid artery stenosis, by diffusion-weighted magnetic resonance imaging (DW-MRI), using the endovascular proximal flow blockage (Mo.Ma device) for cerebral protection.

NCT ID: NCT00795067 Completed - Atherosclerosis Clinical Trials

Relation of Circulating Endothelium-derived Microparticle to Carotid Atherosclerosis

Start date: November 2008
Phase: N/A
Study type: Observational

The investigators hypothesized that circulating endothelium-derived microparticle (EMP) may be a useful surrogate marker of atherosclerosis and future episode of cerebrovascular events. Peripheral blood is drawn at the time of carotid ultrasound examination. Circulating EMPs are counted using flow-cytometry. The correlation among circulating EMP, ultrasound findings, and atherosclerotic risk factors are determined by multiple stepwise regression analysis. The prevalence of cerebrovascular events is also determined during 3-year follow-up period.

NCT ID: NCT00744523 Completed - Clinical trials for Carotid Artery Disease

Proximal Protection With The Mo.Ma Device During Carotid Stenting

ARMOUR
Start date: September 2007
Phase: N/A
Study type: Interventional

The objective of the ARMOUR study is to evaluate the safety and effectiveness of the Mo.Ma proximal flow blockage cerebral protection device for patients at high surgical risk for carotid endarterectomy who undergo carotid artery stenting