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Carotid Stenosis clinical trials

View clinical trials related to Carotid Stenosis.

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NCT ID: NCT00654394 Completed - Clinical trials for Hypercholesterolemia

Progression of Carotid Artery Atheroma in Moderately Hypercholesterolemic Subjects

Start date: January 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to examine the changes in the carotid artery when subjects receive high or low doses of rosuvastatin.

NCT ID: NCT00597974 Completed - Stroke Clinical Trials

Neurological Outcome With Carotid Artery Stenting

CAS
Start date: September 2003
Phase: N/A
Study type: Observational

The purpose of this study is to determine how well patients undergoing carotid artery angioplasty and/or stent-supported angioplasty for the treatment of carotid artery stenosis will perform on a battery of tests to assess brain function before and after the procedure. This study will serve as a pilot project: (a) to determine incidence of neurologic/neuropsychometric change in patients undergoing carotid artery angioplasty and/or stent-supported angioplasty, and (b) to ascertain the time it takes for these changes to resolve.

NCT ID: NCT00597883 Completed - Stroke Clinical Trials

Neuropsychometric Outcome After Carotid Endarterectomy

CEA
Start date: March 2003
Phase: N/A
Study type: Observational

The purpose of this study is to determine how well patients undergoing carotid endarterectomy will perform on a battery of tests to assess brain function before and after surgery as compared to a control group of patients undergoing spine surgery. This study will serve to: (a) determine incidence of neurologic/neuropsychometric change in patients undergoing carotid artery surgery, and (b) to ascertain the time it takes for these changes to resolve.

NCT ID: NCT00597545 Terminated - Diabetes Clinical Trials

Effect of Raised CBF During CEA on Cognition in DM Patients

Start date: March 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if we can reduce the incidence of cognitive dysfunction — difficulty in performing certain pencil-paper, memory, finger dexterity and thinking type of tasks called neuropsychometric tests — in patients with adult onset diabetes mellitus (DM) undergoing surgery on the carotid artery (CEA). We hypothesize that cognitive dysfunction can be decreased in patients with type II DM by augmenting cerebral blood flow with a shunt during carotid endarterectomy compared to patients with Type II DM who are treated with "conventional" management in which a shunt is placed only if the electroencephalogram (EEG) indicates cerebral ischemia.

NCT ID: NCT00594100 Completed - Clinical trials for Carotid Artery Stenosis

GORE Embolic Protection With Reverse Flow

EMPiRE
Start date: July 2006
Phase: Phase 3
Study type: Interventional

To compare the 30-day safety and efficacy of the GORE Flow Reversal System when used with approved carotid stents to an Objective Performance Criterion derived from distal embolic protection studies.

NCT ID: NCT00580580 Withdrawn - Carotid Stenosis Clinical Trials

Detection of Coronary Stenosis With Intravenous Microbubbles

Start date: February 2012
Phase: N/A
Study type: Interventional

To detect coronary artery disease by both coronary and carotid artery imaging and myocardial perfusion imaging using a new low mechanical index real time system.

NCT ID: NCT00536965 Completed - Diabetes Mellitus Clinical Trials

Percentage of Secondary Prevention Patients Treated to Their LDL-C Targets

Start date: July 2007
Phase: N/A
Study type: Observational

A cholesterol/lipid profile screening project of high risk patients with hyperlipidaemia (secondary prevention) who already receive cholesterol-lowering therapy. Lipid profile and rate of patients who are treated to target (which is <100mg/dl for patients with high risk and <70mg/dl for patients at very high risk) are screened (office-based specialists). The doctors therapy decisions after the screening and possible reasons for these decisions will be documented. Our aim is to evaluate dosing habits, to evaluate how many patients are treated to their LDL-C target and to underline the importance of treating patients to their cholesterol targets.

NCT ID: NCT00536796 Completed - Diabetes Mellitus Clinical Trials

Percentage of Secondary Prevention Patients Treated to Their LDL-C Targets

Start date: September 2007
Phase: N/A
Study type: Observational

A cholesterol/lipid profile screening project of high risk patients with hyperlipidaemia (secondary prevention) who already receive cholesterol-lowering therapy. Lipid profile and rate of patients who are treated to target (which is <100mg/dl for patients with high risk and <70mg/dl for patients at very high risk) are screened (hospital-based specialists). The doctors therapy decisions after the screening and possible reasons for these decisions will be documented. Our aim is to evaluate dosing habits, to evaluate how many patients are treated to their LDL-C target and to underline the importance of treating patients to their cholesterol targets.

NCT ID: NCT00514644 Completed - Carotid Stenoses Clinical Trials

Stroke and Panorama - Analyzing Carotid Endocalcifications (SPACE)

SPACE
Start date: August 2007
Phase: N/A
Study type: Interventional

The odontological radiology method Panorama is known to be able to spot calcifications in the area of the carotid arteries. The calcifications could be carotid stenoses which is affiliated with an increased risk of stroke. The study aims to investigate if panorama examinations can be used as a starting point for further investigation of the carotid arteries.

NCT ID: NCT00514592 Completed - Carotid Stenoses Clinical Trials

Additional Neurological Symptoms Before Surgery of the Carotid Arteries - A Prospective Study (ANSYSCAP)

ANSYSCAP
Start date: August 2007
Phase: N/A
Study type: Observational

A single center observational study. Observing the time between cerebrovascular symptoms and Carotid Endarterectomy (CEA) and patient outcome. An intervention at 17 of the 29 study months aimed at reducing the delay and increasing the patient safety. Main outcome is to measure the reduction in recurrent stroke with decreased delay to CEA.