Evaluation of Cerebrovascular Events in Patients With Occlusive Carotid Artery Disorders

NCT ID: NCT03840265

Last Updated: 2020-03-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-02-06

Study Completion Date

2022-11-30

Brief Summary

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As of today, no suitable multiparametric predictive method is available to properly estimate stroke risk in patients with carotid artery stenosis. Carotid artery stenosis is one of the proven risk factors of stroke incidence, but the indication of its intervention is merely the grade of stenosis itself. The current international guidelines suggest intervention for asymptomatic patients only with potentially high risk plaques but pharmacological treatment is advised to low risk patients. Unfortunately there is no proven and widely accepted system to distinguish these two categories of patients with carotid artery stenosis.

In this project the following parameters will be assessed both in asymptomatic and symptomatic patients: 1, preoperative stroke risk prediction based on comparative analysis of CT angiography (CTA) results of plaque morphology and ultrasound (US) based plaque elastography analysis, 2) intracranial bloodflow will be measured by transcranial Doppler sonography(TCD), 3) presence recent of silent brain ischemia on diffusion weighted imaging (DWI) MR (magnetic resonance), 4) retinal perfusion measurement by optical coherence tomography angiography (OCT). The investigators aim to establish a clinically meaningful and more accurate (than stenosis grade) stroke risk prediction algorithm for asymptomatic carotid stenosis patients based on these parameters.

Detailed Description

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Stroke is one of the leading causes of mortality in Hungary. While stroke mortality is 8-10/100.000 in the population under 50 years of age in Western European countries, the mortality is 40/100.000 in women and 60/100.000 in men in Hungary. In the investigators' country the stroke patients are 5-10 years younger as compared to other developed countries. The total stroke mortality in the first 24 months in Hungary is approximately 30%, furthermore 32-42% of the survivors need permanent help in completing their daily routine tasks. Carotid artery disease of atherosclerotic origin is common in the elderly population. The cause of cerebral ischemia in approximately half of the patients is due to the rupture of atherosclerotic plaque with subsequent embolization of thrombus and/or plaque material in the cerebral circulation. Prevention of cerebral ischemia is the goal of pharmacological or surgical treatment. The decision for surgical treatment such as carotid endarterectomy (CEA) or carotid artery stenting (CAS) is based on the degree of stenosis, but incorporating non-invasive measures of plaque composition is expected to improve the selection of patients that will benefit from surgical intervention. The number of asymptomatic patients with carotid stenosis needed to treat to prevent one stroke with endarterectomy is 20, which is quite high compared to 8 in the symptomatic patient group. There is a clear need to identify asymptomatic individuals at high risk of developing future ischemic events to avoid unnecessary surgery. It has been remarked, that the recent AHA (American Heart Association) guideline on the management of significant asymptomatic carotid stenosis recommends that surgery may be considered in highly selected patients. However, no guidance was provided as to which patient is the "highly selected" one.

As of today, no suitable predictive method is available to properly estimate stroke risk in patients with carotid artery stenosis. Carotid artery stenosis is one of the proven risk factors of stroke incidence, but the indication of its intervention is merely the grade of stenosis itself. The current international guidelines suggest intervention for asymptomatic patients only with potentially high risk plaques, but pharmacological treatment is advised for low risk patients. Unfortunately there is no proven and widely accepted system to distinguish these two categories of patients with carotid artery stenosis.

Aims:

The investigators' aim is to establish a stroke risk prediction score system -based on CTA and US plaque morphology and blood sample biomarkers- for asymptomatic carotid artery stenosis patients. A more specific and more accurate system -than the currently applied stroke risk score systems- would allow for the selection of the potentially high risk plaques in asymptomatic patients with borderline grade stenosis.These patients would benefit more from surgical treatment while asymptomatic patients with low risk plaques could avoid the risk of an invasive treatment.

1. Morphological features related to surgical related cerebrovascular events: The investigators plan to overview the clinical records retrospectively to find morphological, hemodynamical and clinical predictors of intra- and early postoperative cause of the cerebrovascular events. An isolated middle cerebral artery carries higher risk of immediate neurological event after carotid endarterectomy with cross-clamping without shunt protection. This project's secondary aims are the following: to compare the accuracy of the CTA and MR imaging in the assessment of the Circle of Willis (CoW) morphology in all patients before CEA and to evaluate changes in CoW morphology before and after CEA, to compare ischemic changes before and after CEA regarding CoW morphology, shunt usage and to evaluate the impact of contralateral carotid occlusion on immediate neurological event (INE) regarding CoW and other supra-aortic morphology. Retrospective assessment of the correlation between intracranial vascular morphology with CTA and intraoperative stroke risk would provide help in perioperative stroke risk prediction and planning of optimal surgical technique.
2. Micro-embolization and carotid plaque analysis: The investigators aim is to define a group of patients in the study cohort, who are clinically asymptomatic, but suffered silent brain ischemia (SBI) before surgery, and to analyze their plaque using a dedicated software for plaque assessment (Medis QAngioCT) and compare to asymptomatic without SBI and symptomatic patients plaques. In Hungary the gold standard of the preoperative imaging of carotid artery stenosis in asymptomatic and symptomatic patients is CTA. These images can be used for plaque analysis that is to identify vulnerable plaque morphology in coronary arteries. The identification of preoperative plaque vulnerability based on the comparison of the ultrasound plaque elastography and contrast enhanced plaque analysis, the transcranial Doppler ultrasound (which can detect microembolisation), cranial DWI-MR for verification of silent recent ischaemic lesions and the histopathology of surgically removed plaques with CTA and US based plaque morphology can define vulnerable plaques related to adverse events.
3. Evaluation of retinal perfusion changes following carotid interventions using OCT angiography in patients with carotid stenosis to assess the influence of carotid stenting and carotid endarterectomy on retinal perfusion using OCTA in patients with significant carotid artery stenosis. Furthermore, this study evaluates the predictive accuracy of retinal microvasculature alterations on the development of postoperative stroke. Carotid artery occlusive disease may result in different vision threatening ocular manifestations, for instance, retinal vascular occlusions and ocular ischemic syndrome (OIS). The diagnosis of carotid stenosis is critical as it is an important risk factor of serious cerebrovascular disease. OCT angiography could be a useful non-invasive method for early diagnosis of patients with carotid stenosis and to evaluate the outcome of carotid interventions. Better identification of patients with carotid stenosis is crucial for the prevention of vision loss and stroke.

Conditions

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Carotid Stenosis Carotid Artery Plaque Cerebrovascular Embolism and Thrombosis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Carotid endarterectomy

All patients in this study will undergo carotid endarterectomy procedure

Group Type OTHER

carotid endarterectomy

Intervention Type PROCEDURE

In this project the following parameters will be assessed both in asymptomatic and symptomatic patients underwent carotid endarterectomy: 1) hemodynamic modeling of effect of the supraaortic arteries anatomic variations and pathologies 2, preoperative stroke risk prediction based on comparative analysis of CTA results of plaque morphology and ultrasound-based plaque elastography analysis, 3) cerebral flow measurement by transcranial Doppler sonography(TCD), 4) presence recent of silent brain ischemia on DWI-MRI, 5) OCT angiography could be a useful non-invasive method for evaluation of the outcome of carotid interventions

Interventions

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carotid endarterectomy

In this project the following parameters will be assessed both in asymptomatic and symptomatic patients underwent carotid endarterectomy: 1) hemodynamic modeling of effect of the supraaortic arteries anatomic variations and pathologies 2, preoperative stroke risk prediction based on comparative analysis of CTA results of plaque morphology and ultrasound-based plaque elastography analysis, 3) cerebral flow measurement by transcranial Doppler sonography(TCD), 4) presence recent of silent brain ischemia on DWI-MRI, 5) OCT angiography could be a useful non-invasive method for evaluation of the outcome of carotid interventions

Intervention Type PROCEDURE

Other Intervention Names

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Cranial MR Transcranial Doppler Ultrasound Optical coherence tomography angiography Carotid CT angiography

Eligibility Criteria

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Inclusion Criteria

* signed informed consent,
* significant carotid artery stenosis

Exclusion Criteria

* Age under 50 years
* Neurological event 15 days before operation
* Chronic kidney disease
* Pacemaker or ICD implantation
* Atrial fibrillation
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Research, Development and Innovation Office

UNKNOWN

Sponsor Role collaborator

Semmelweis University Heart and Vascular Center

OTHER

Sponsor Role lead

Responsible Party

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Prof. Dr. Sótonyi Péter

MD, PhD, Head of Vascular Surgery Department of Semmelweis University

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Péter Sótonyi, MD PhD

Role: STUDY_DIRECTOR

Semmelweis University Heart and Vascular Centre

Locations

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Semmelweis University Heart and Vascular Centre

Budapest, Budapest XII, Hungary

Site Status RECRUITING

Countries

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Hungary

Central Contacts

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Zsuzsanna Mihály, MD

Role: CONTACT

+36-20-666-3673

Claudia Halász

Role: CONTACT

+36-20-666-3227

Facility Contacts

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Zsuzsanna Mihály

Role: primary

+36-20-666-3673

Other Identifiers

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SemmelweisUHVC

Identifier Type: -

Identifier Source: org_study_id

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