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Prognostic Value of Carotid CEUS in Acute Ischemic Stroke Patients

Seoul National University logo

Seoul National University

Status

Unknown

Conditions

Ischemic Stroke
Carotid Stenosis
Ultrasonography

Study type

Observational

Funder types

Other

Identifiers

NCT03283306
B-1607-356-304

Details and patient eligibility

About

Contrast-enhanced ultrasound(CEUS) of carotid artery plaque is a novel method that enabled direct visualization of neovessels in the vulnerable plaque. Plaque enhancement with CEUS showed correlation with the histologic density of neovessels within the carotid plaque and the previous cardiovascular events. Vulnerable plaques with a high risk of thromboembolic complications and rapid progression is associated with acute ischemic stroke. The prognostic value of vulnerable carotid artery plaque depicted with CEUS has not been fully investigated. The purpose of this study is to define prognostic value of plaque enhancement on carotid CEUS in acute stroke patients. Research question is; in acute ischemic stroke patients with ipsilateral carotid plaque as probable etiology of stroke, is the presence of carotid plaque enhancement on CEUS independent predictor of future stroke.

Enrollment

667 estimated patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients older than 19 years presenting acute ischemic stroke.
  2. Compatible neurologic symptom within 14 days
  3. Compatible MRI finding (one or more positive DWI lesions in the territory of unilateral ICA: ACA or MCA territory) - interpretable MRI image obtained in SNUBH or outside hospital
  4. Etiology of acute ischemic stroke: except cardioembolic stroke (Atrial fibrillation) and other determined etiology
  5. Ipsilateral extracranial carotid artery stenosis on MRA (CE-MRA), CTA or Doppler ultrasound

Exclusion criteria

  1. History of ipsilateral carotid stent or endarterectomy
  2. Carotid intervention during hospital stay
  3. Contraindication to ultrasound contrast agent (SonoVue) A. Right to left, bi-directional, or transient right to left cardiac shunts B. History of hypersensitivity reactions to sulfur hexafluoride lipid microsphere components or any ultrasound contrast agent C. Pregnant or lactating woman D. Unstable cardiopulmonary conditions (acute myocardial infarction, acute coronary artery syndromes, worsening congestive heart failure, or serious ventricular arrhythmias)
  4. Expected life span less than 12 months

Trial contacts and locations

1

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Central trial contact

Eun Jung Kim; Yeo Koon Kim, MD

Data sourced from clinicaltrials.gov

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