Ultrafast Ultrasound Imaging Assesment of Carotid Plaque Neovascularization

NCT ID: NCT04470687

Last Updated: 2024-07-11

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

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-17

Study Completion Date

2022-09-15

Brief Summary

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Stroke is the second leading cause of death in the Western world and the leading cause of major lifelong disability. About 15% of strokes are secondary to thrombosis or embolization of an unstable atheromatous carotid plaque. In these symptomatic patients, the degree of carotid stenosis is correlated with the risk of early recurrence. Patients with stenosis over 70% are therefore offered an endarterectomy, an operation to remove carotid plaque, to prevent future strokes\[1\]. In asymptomatic patients, the degree of stenosis is a limited predictor, and better risk stratification is required to assess the degree of plaque vulnerability and stroke risk of the patient. The therapeutic decision towards endarterectomy in addition to drug therapy is debated because of a variable and dependent benefit/risk balance for each patient. A number of imaging parameters have been studied: ulceration, heterogeneity, vascularization of the plaque for example, but their place is not well defined \[2\].

The usual evaluation of carotid stenosis is by conventional Doppler ultrasound with calculation of the degree of stenosis according to the NASCET criteria.

For symptomatic stenoses the intervention is recommended when above 70% and is discussed from 50% to 70% of NASCET stenosis degree.

For asymptomatic stenoses, the procedure is discussed when above 60% taking into account the patient's life expectancy, the risk of the surgery and the unstable nature of the plaque \[2\].

Destabilization of the carotid plaque is partially induced by inflammation associated with neo-vascularization. The detection of these new vessels by conventional contrast ultrasound has already shown a distinction between stable and unstable plaques, by the presence or absence of microbubbles in the plaque. However, this assessment is not very precise and only the most vascularized plaques can be detected. Ultrafast ultrasound Imaging is a new ultrasonic Imaging modality that allows detecting low speed flows, a tiny vascular structure within the vessel wall.

RESEARCH HYPOTHESIS Plaques neo-vascularization would be more precisely detected and characterized by ultrafast imaging coupled with microbubble injection than conventional ultrasound imaging.

A better assessment of plaque instability could improve the selection of patients for carotid endarterectomy and increase the benefit/risk ratio of this preventive surgery.

Detailed Description

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see above

Conditions

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Carotid Stenosis Carotid Artery Diseases Carotid Atherosclerosis Carotid Artery Plaque Atheroma; Carotid Artery

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 plaque or stenosis ultrasound enhanced UF assesment

symptomatic or asymptomatic patients with atheromatous carotid stenosis scheduled for carotid endarterectomy

Group Type EXPERIMENTAL

contrast enhanced ultrafast ultrasound imaging

Intervention Type DEVICE

Ultrasound contrast medium: SonoVue 8µL/mL (Bracco International BV) Ultrasound scanner: Aixplorer® device marketed by SuperSonic Imagine©, CE Doppler UltraFast™Doppler, contrast ultrasound (CEUS), color Doppler and ultra-sensitive energy Doppler, high-performance directional energy Doppler, Elastography ShearWave™ UF-Doppler (UltraFast-Doppler) and microbubble injection (SonoVue) Apparatus for performing the UF Doppler sequence: Aixplorer, manufacturer : Supersonic Imagine, Aix-en-Provence, France, CE Marking.

3D RCA dedicated vascular probe with dedicated Doppler sequences

Interventions

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contrast enhanced ultrafast ultrasound imaging

Ultrasound contrast medium: SonoVue 8µL/mL (Bracco International BV) Ultrasound scanner: Aixplorer® device marketed by SuperSonic Imagine©, CE Doppler UltraFast™Doppler, contrast ultrasound (CEUS), color Doppler and ultra-sensitive energy Doppler, high-performance directional energy Doppler, Elastography ShearWave™ UF-Doppler (UltraFast-Doppler) and microbubble injection (SonoVue) Apparatus for performing the UF Doppler sequence: Aixplorer, manufacturer : Supersonic Imagine, Aix-en-Provence, France, CE Marking.

3D RCA dedicated vascular probe with dedicated Doppler sequences

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* The patient is over 18
* The patient is scheduled for carotid endarterectomy within 30 days at most
* The patient has a social security system

Exclusion Criteria

* Non-atheromatous carotid stenosis (radiation)
* Contraindication of the use of SonoVue ultrasound contrast media. Hypersensitivity to the active ingredient or any of the following excipients: Macrogol 4000; Distearoylphosphatidylcholine; Dipalmitoylphosphatidylglycerol sodium; Palmitic acid.
* The patient has any of the following conditions: right-left shunt, severe pulmonary hypertension (pulmonary blood pressure \> 90 mm Hg), uncontrolled systemic hypertension and respiratory distress syndrome.
* Lack of social security coverage, patient under justice
* Allergy to ultrasound gel
* Pregnancy. (As a precautionary measure, it is best to avoid using SonoVue during pregnancy according to SPC)
* Patient under guardianship or curatorship or under the protection of justice.
* Patient unable or unwilling to give written consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Institut National de la Santé Et de la Recherche Médicale, France

OTHER_GOV

Sponsor Role collaborator

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Tristan MIRAULT, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Hopital europeen Georges-Pompidou

Locations

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Hopital europeen Georges-Pompidou

Paris, , France

Site Status

Countries

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France

Other Identifiers

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2019-A03331-56

Identifier Type: OTHER

Identifier Source: secondary_id

APHP180482

Identifier Type: -

Identifier Source: org_study_id

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