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Carotid Artery Stenosis clinical trials

View clinical trials related to Carotid Artery Stenosis.

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NCT ID: NCT02802072 Completed - Clinical trials for Carotid Artery Stenosis

Enterprise Stent Implantation in the Treatment of Carotid Artery Stenosis With Ischemic Stroke

Start date: January 2013
Phase: N/A
Study type: Interventional

To investigate the long-term effects of intracranial implantation of Enterprise stent system versus antiplatelet medication on neurologic deficits, daily living abilities, and carotid artery stenosis in patients with atherosclerotic ischemic stroke.

NCT ID: NCT02800174 Completed - Clinical trials for Carotid Artery Stenosis

Smart Nitinol Stent System for the Treatment of Severe Atherosclerotic Carotid Stenosis

Start date: June 2006
Phase: N/A
Study type: Interventional

To validate the long-term effects of implantation of the self-expanding Smart nitinol stent system for the treatment of severe atherosclerotic carotid stenosis in a 2-year follow-up study of a large patient cohort

NCT ID: NCT02689414 Completed - Clinical trials for Peripheral Artery Disease

A Study of Remote Ischaemic Preconditioning in Patients With Atherosclerosis Undergoing Vascular Surgery

Start date: January 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of preoperative remote ischaemic preconditioning (RIPC) on organ damage and the functional characteristics of arteries in patients undergoing vascular surgery. In addition, we investigate the connection between RIPC and changes in the functional characteristics of arteries and low molecular weight metabolites.

NCT ID: NCT02677545 Completed - Clinical trials for Carotid Artery Stenosis

Ticagrelor Versus Clopidogrel in Carotid Artery Stenting

PRECISE-MRI
Start date: December 2016
Phase: Phase 2
Study type: Interventional

Patients with symptomatic or asymptomatic carotid stenosis in whom carotid artery stenting is planned are randomised between antiplatelet therapy with ticagrelor plus aspirin or clopidogrel plus aspirin and examined with brain MRI before and after stent treatment. The proportion of patients with new ischaemic lesions on MRI after treatment is compared between the two groups.

NCT ID: NCT02629653 Completed - Stroke Clinical Trials

Body Cooling During Carotid Endarterectomy: No-profit, Open, Mono-centric, Feasibility Study

Start date: December 2013
Phase: N/A
Study type: Interventional

Aim of the study is to determine whether endovascular systemic cooling to a target temperature of 34-35°C initiated before, and maintained during Carotid EndoArterectomy (CEA), is feasible and safe

NCT ID: NCT02450734 Completed - Clinical trials for Carotid Artery Stenosis

Ultrasound-guided Intermediate Cervical Plexus Block for Carotid Surgery

Start date: April 2011
Phase: N/A
Study type: Observational

Since stroke and myocardial ischemia are major causes of perioperative morbidity and mortality associated with carotid endarterectomy, monitoring the brain and ensuring the best hemodynamic stability are important goals of perioperative management. The investigators conducted a prospective observational study about efficacy and safety of the ultrasound-guided intermediate cervical plexus block (CPB), with early (immediate postoperative) and mid-term (day 30) outcomes in awake patients undergoing carotid endarterectomy.

NCT ID: NCT02341196 Completed - Stroke Clinical Trials

Randomized Clinical Trial of Polyester vs. Polyurethane Patch for Carotid Endarterectomy

Start date: January 1995
Phase: N/A
Study type: Interventional

This study examines the risk of thrombogenicity of the carotid patches in polyurethane compared to carotid patches in polyester including death, any stroke, carotid thrombosis at 30 days and long-term results including stroke and recurrent carotid stenosis at 10 years. This study was run at the University of Roma, La Sapienza and at the University of Poitiers, randomisation was done in both enters after approval by the Ethical committee of the University of Roma (Record uploaded)

NCT ID: NCT02006095 Completed - Clinical trials for Carotid Artery Stenosis

Neuroimaging Correlates of Memory Decline Following Carotid Interventions

Start date: November 2012
Phase:
Study type: Observational

Carotid revascularization can significantly reduce the risk of stroke in patients with severe carotid stenosis; however, it has been associated with cognitive decline in 25% of the older adults who undergo the procedure. Characterizing risk factors for cognitive decline following carotid interventions and individualizing treatment strategy based on those risks can minimize procedure-associated cognitive dysfunction. Neuroimaging techniques that characterize white matter integrity and regional hypoperfusion have the potential to provide sensitive brain structure indicators that may be associated with memory decline following revascularization procedures. In this protocol, we hope to determine how cerebral blood flow and baseline white matter abnormality in the vulnerable region modify the frequency and cognitive effect of microembolization following carotid revascularization procedures.

NCT ID: NCT01901874 Completed - Clinical trials for Carotid Artery Stenosis

The Gore SCAFFOLD Clinical Study

Start date: July 2013
Phase: N/A
Study type: Interventional

Evaluate the safety and efficacy of the GORE® Carotid Stent for the treatment of carotid artery stenosis in patients at increased risk for adverse events from carotid endarterectomy

NCT ID: NCT01718600 Completed - Clinical trials for Carotid Artery Stenosis

Long-term Neurocognitive Sequelae of Subclinical Microembolization During Carotid Interventions

Start date: June 2011
Phase:
Study type: Observational

Microembolization is commonly associated with carotid artery stenting (CAS), but our understanding of subclinical microembolization is superficial. Through collaborative effects of multidisciplinary team-experts, novel approaches, and longitudinal evaluations, we hope to better understand the clinical significance and long-term cognitive effects of microemboli. This proposal may change our current clinical practice by providing a better outcome measure for carotid interventions and improving outcomes of CAS procedures through risk factor stratification. Our central hypothesis is that development of subclinical microemboli is associated with decline in cognitive function following CAS and that the risk of development of microemboli themselves is associated with patient- and procedure-related factors. We hope that this prospective study will help to clarify these important issues in the era of rapidly evolving percutaneous interventions.