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Carotid Artery Diseases clinical trials

View clinical trials related to Carotid Artery Diseases.

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NCT ID: NCT01893489 Completed - Atherosclerosis Clinical Trials

Visualization of Carotid Atherosclerosis by 68Ga-MSA

Start date: September 2012
Phase: Phase 1
Study type: Interventional

Until now, no specific atherosclerosis-targeting agent labeled with positron emitter is not yet available. Investigators developed neomannosyl human serum albumin(MSA) for the terminal mannose residues of MSA binding with the mannose receptors of macrophages in atherosclerosis, and investigators investigate whether 68Ga-MSA can be a novel agent for non-invasive molecular imaging of carotid atherosclerotic lesion in PET.

NCT ID: NCT01783639 Completed - Stroke Clinical Trials

Safety and Performance Evaluation of WIRION™ EPD in Patients Undergoing Carotid Artery Stenting

WISE
Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the safety and performance of WIRION™ EPD in patients undergoing carotid artery stenting to a performance goal based on an analysis of the results of previous US IDE carotid stenting with embolic protection studies

NCT ID: NCT01743404 Recruiting - Clinical trials for Carotid Atherosclerosis

Study of Anti-atherosclerotic Activity of Inflaminat in Asymptomatic Participants With Subclinical Atherosclerosis

Start date: September 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the anti-atherosclerotic effect of long-term anti-inflammatory therapy (Inflaminat) in asymptomatic participants with subclinical atherosclerosis of carotid arteries.

NCT ID: NCT01742845 Completed - Clinical trials for Carotid Atherosclerosis

Ultrasound-guided Intermediate Cervical Block Versus Superficial Cervical Block for Carotid Endarterectomy (CERVECHO)

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

The aim of this prospective, randomised, controlled study is to compare the efficacy of ultrasound-guided intermediate cervical block to superficial block for carotid endarterectomy. Patients scheduled for carotide endarterectomy under regional anaesthesia (ropivacaine 4.75 mg/ml) are randomised into 2 groups according to the technique of anaesthesia performed: superficial cervical block (Control group) or, ultrasound guided intermediate cervical block (Echo group). Main outcome is cervical block success, defined by surgery performed under regional anaesthesia without supplemental topical lidocaine. Secondary outcomes are rate of conversion to general anaesthesia, total dose of supplemental topical lidocaine and block-related complications.

NCT ID: NCT01734707 Completed - Clinical trials for Carotid Atherosclerosis

Atherosclerosis Monitoring and Atherogenicity Reduction Study

Start date: January 2004
Phase: Phase 3
Study type: Interventional

This study was designed to estimate the effect of two-year treatment with time-released garlic-based drug Allicor on the progression of carotid atherosclerosis in double-blinded placebo-controlled randomized clinical trial.

NCT ID: NCT01701830 Recruiting - Atherosclerosis Clinical Trials

Serum Omentin-1 and Carotid Atherosclerosis In Non-Diabetic Chronic Kidney Disease

Start date: October 2012
Phase: N/A
Study type: Observational

The aim of the study is to evaluate whether a low level of serum omentin-1 is associated with carotid atherosclerosis and mediated by inflammation.

NCT ID: NCT01691911 Completed - Clinical trials for Abdominal Aortic Aneurysm

Preconditioning Shields Against Vascular Events in Surgery

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

Major vascular surgery involves operations to repair swollen blood vessels, clear debris from blocked arteries or bypass blocked blood vessels. Patients with these problems are a high-risk surgical group as they have generalized blood vessel disease. These puts them at risk of major complications around the time of surgery such as heart attacks , strokes and death. The mortality following repair of a swollen main artery in the abdomen is about 1 in 20. This contrasts poorly with the 1 per 100 risk of death following a heart bypass. Simple and cost-effective methods are needed to reduce the risks of major vascular surgery. Remote ischaemic preconditioning (RIPC) may be such a technique. To induce RIPC, the blood supply to muscle in the patient's arm is interrupted for about 5 minutes. It is then restored for a further five minutes. This cycle is repeated three more times. The blood supply is interrupted simply by inflating a blood pressure cuff to maximum pressure. This repeated brief interruption of the muscular blood supply sends signals to critical organs such as the brain and heart, which are rendered temporarily resistant to damage from reduced blood supply. Several small randomized clinical trials in patients undergoing different types of major vascular surgery have demonstrated a potential benefit. This large, multi-centre trial aims to determine whether RIPC can reduce complications in routine practice.

NCT ID: NCT01685567 Completed - Clinical trials for Carotid Artery Disease

Safety and Efficacy Study for Reverse Flow Used During Carotid Artery Stenting Procedure

ROADSTER
Start date: November 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the MICHI™ Neuroprotection System with Filter (MICHI™ NPS+f) in providing cerebral embolic protection during carotid artery stenting. It will be used in conjunction with a FDA approved carotid artery stent for the treatment of carotid artery disease.

NCT ID: NCT01640613 Completed - Clinical trials for Regional Anesthesia Morbidity

Anterior Ultrasound-guided Cervical Plexus Block for Carotid Endarterectomy

Start date: April 2012
Phase: N/A
Study type: Observational

The aim of this study is to describe technique, efficiency, safety and satisfaction of ultrasound guided intermediate cervical plexus block for carotid endarterectomy. The investigators present a simple approach for carotid regional anaesthesia by an anterior way that has not been published yet.

NCT ID: NCT01608516 Recruiting - Inflammation Clinical Trials

Multimodal Imaging Assessment of the Inflammatory Atheromatous Plaque

Start date: April 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The present study aims at assessing the ability of 68Ga-NODAGA-RGD PET/CT for the detection of inflammatory atheromatous plaques in the carotid arteries, compared to 18F-FDG PET/CT, MRI and US and to determine the contribution of each imaging technique. Current gold standard for inflammation is histopathology. Hypothesis : 68Ga-NODAGA-RGD might give a better initial evaluation of patients with atheromatous plaques in the carotid artery eligible for endarterectomy.