Morphology of Advanced Symptomatic Cerebral Plaques With High Embolic Potential

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age30-85
SponsorChinese University of Hong Kong

About this trial

The study is to attain early recognition of the unstable plaques which have an imminent embolic risk in patients with intracranial atherosclerotic disease (IAD).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient is 30 to 85 years of age, inclusive.

Patients who have an acute infarct in diffusion-weighted MRI compatible with artery-to-artery thrombo-embolism, a relevant intracranial atherosclerotic stenosis ≥60%, and MES detected by TCD.

Patient who has no contra-indication for the proposed imaging tests.

Patient understands the purpose and requirements of the study, and has provided an informed consent.

Disqualifiers

Stroke etiology uncertain or unrelated to intracranial atherosclerosis, such as cardioembolism, Moyamoya disease, small vessel disease, etc.

A tandem stenosis >50% at proximal internal carotid artery.

Bleeding propensity: active peptic ulcer disease, major systemic hemorrhage within 30 days, thrombocytopenia (platelets <100 x 109/L), coagulopathy (INR >1.5).

A medical condition that would not allow the patient to adhere to the protocol or complete the study.

Trial population

Patients who admitted to Prince of Wales Hospital for acute stroke will be screened for eligibility.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • DSA/3DRA

    Diagnostic test

    DSA/3DRA

Treatment groups

140 Participants
are divided into 2 treatment groups
Group A: Symptomatic stroke patient1 intervention
Group B: Asymptomatic stroke patient1 intervention

Trial outcomes

Primary outcomes

1

The plaque morphology of high-risk IAD may be distinct from the silent ones.

The morphological attributes (surface outline, angulations and plaque volume) and collateral grading will be compared between symptomatic and asymptomatic group.

Time frame
Dec, 2020

Secondary outcomes

Other outcomes

Sponsors and contacts

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