Transcutaneous ARFI Ultrasound for Differentiating Carotid Plaque With High Stroke Risk

NCT ID: NCT04063709

Last Updated: 2025-02-07

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-07-17
• Study Completion Date: 2025-11-30

Brief Summary

Stroke is a leading cause of death and disability in the United States and around the world. The goal of this work is to develop and test a noninvasive ultrasound-based imaging technology to better identify patients at high risk of stroke so that appropriate and timely intervention may be administered to prevent it.

Detailed Description

Although stroke remains a leading cause of death in the United States, incidence and mortality rates have declined over the past two decades in association with advanced pharmaceutical therapies and revascularization, primarily by carotid endarterectomy (CEA). While CEA's efficacy for preventing stroke in patients with severe (≥70%) carotid artery stenosis and neurological symptoms is well documented, the surgical intervention's usefulness decreases as stroke risk falls in patients with less severe stenosis and patients without symptoms. It is estimated that as many as 13 out of 14 symptomatic patients with 50-69% stenosis and 21 out of 22 asymptomatic patients with 70-99% stenosis undergo CEA surgery unnecessarily. These data demonstrate the inadequacy of degree of stenosis as the primary indication of stroke risk and underscore the urgent yet unmet need for improved biomarkers that differentiate patients at low risk of embolic stroke from those in need of CEA to prevent it.

This urgent need for improving CEA indication could be met by assessing the structure and composition of carotid plaques. Plaques composed of thin or ruptured fibrous caps (TRFC), large lipid rich necrotic cores (LRNC), and intraplaque hemorrhage (IPH) are associated with thrombosis in morphological studies from autopsy. Further, plaque hemorrhage and increased intraplaque vessel formation in CEA specimens are independently related to future cardio- and cerebrovascular events or interventions. Finally, previous stroke or transient ischemic attack (TIA) is associated with TRFC and IPH - while increased risk of future stroke or TIA is conferred by TRFC, LRNC, and IPH - in human carotid plaques as determined by in vivo magnetic resonance imaging (MRI).

The goal of this work is to develop a low-cost, noninvasive imaging method that reliably delineates carotid plaque structure and composition and is suitable for widespread diagnostic application. Previous research has demonstrated that Acoustic Radiation Force Impulse (ARFI) ultrasound delineates LRNC/IPH, collagen/calcium deposits, and TRFC in human carotid plaque, in vivo, with TRFC thickness measurement as low as 0.49 mm - the mean thickness associated with rupture. This project will exploit ARFI Variance of Acceleration (VoA) imaging, higher center frequencies, and harmonic imaging to newly enable separate discrimination of TRFC, LRNC, and IPH and accurate feature size measurement. The investigators will determine the association between advanced ARFI's plaque characterization and recent history of ipsilateral stroke or TIA.

Conditions

Plaque, Atherosclerotic; Carotid Artery Plaque; Carotid Stenosis

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Symptomatic with 50-69% stenosis

Patients 18 years of age or older who have been selected by their treating physician to be in need of carotid revascularization by CEA, with 50-69% stenotic carotid plaque with associated neurological symptoms. Acoustic Radiation Force Impulse (ARFI) ultrasound imaging will be performed on the carotid plaque.

Group Type: EXPERIMENTAL

Acoustic Radiation Force Impulse (ARFI) ultrasound

Intervention Type: DIAGNOSTIC_TEST

ARFI imaging is an ultrasound-based, noninvasive imaging method and will be used in accordance with approved labeling.

Symptomatic with 70-99% stenosis

Patients 18 years of age or older who have been selected by their treating physician to be in need of carotid revascularization by CEA, with 70-99% stenotic carotid plaque with associated neurological symptoms. ARFI ultrasound imaging will be performed on the carotid plaque.

Group Type: EXPERIMENTAL

Acoustic Radiation Force Impulse (ARFI) ultrasound

Intervention Type: DIAGNOSTIC_TEST

ARFI imaging is an ultrasound-based, noninvasive imaging method and will be used in accordance with approved labeling.

Asymptomatic with 70-99% stenosis

Patients 18 years of age or older who have been selected by their treating physician to be in need of carotid revascularization by CEA, with 70-99% stenotic carotid plaque without associated neurological symptoms. ARFI ultrasound imaging will be performed on the carotid plaque.

Group Type: EXPERIMENTAL

Acoustic Radiation Force Impulse (ARFI) ultrasound

Intervention Type: DIAGNOSTIC_TEST

ARFI imaging is an ultrasound-based, noninvasive imaging method and will be used in accordance with approved labeling.

Asymptomatic with 50-69% stenosis

Patients 18 years of age or older who have been diagnosed with 50-69% carotid artery stenosis without clinical indication for CEA.

Group Type: EXPERIMENTAL

Acoustic Radiation Force Impulse (ARFI) ultrasound

Intervention Type: DIAGNOSTIC_TEST

ARFI imaging is an ultrasound-based, noninvasive imaging method and will be used in accordance with approved labeling.

Interventions

Acoustic Radiation Force Impulse (ARFI) ultrasound

ARFI imaging is an ultrasound-based, noninvasive imaging method and will be used in accordance with approved labeling.

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

1. aged 18 years or older

2. having 50-99% stenotic symptomatic carotid plaque with clinical indication for endarterectomy

3. having 50-69% stenotic asymptomatic carotid plaque without clinical indication for endarterectomy

Exclusion Criteria

1. prior CEA or carotid stenting

2. carotid occlusion

3. vasculitis

4. malignancy

5. inability to provide informed consent

6. prior radiation therapy to the neck

7. treatment with immunomodulating drugs

8. oncological disease.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)

NIH

Sponsor Role: collaborator

University of North Carolina, Chapel Hill

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Caterina Gallippi, PhD

Role: PRINCIPAL_INVESTIGATOR

UNC Chapel Hill

Locations

The University of North Carolina at Chapel Hill Hospitals

Chapel Hill, North Carolina, United States

Countries

United States

Other Identifiers

R01HL092944-06A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

17-2700

Identifier Type: -

Identifier Source: org_study_id