Skip to content

A cohort study on the identification and outcome evaluation of intracranial arteriosclerosis plaque vulnerability

A cohort study on the identification and outcome evaluation of intracranial arteriosclerosis plaque vulnerability

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105624
Enrollment
Unknown
Registered
2025-07-08
Start date
2025-01-03
Completion date
Unknown
Last updated
2025-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asymptomatic intracranial atherosclerosis

Interventions

Observation group:None

Sponsors

Xuanwu Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Asymptomatic intracranial atherosclerosis patients: (1) Age 30-80 years; (2) TCD-proven intracranial artery stenosis with atherosclerosis as clinically considered; (3) No history of stroke or transient ischemic attack; (4) The temporal window has good sound permeability; (5) Sign the informed consent form. 2. Patients with asymptomatic severe stenosis: (1) Age 30-80 years; (2) Willis circumferential intracranial atherosclerotic stenosis (>70% or occlusion), confirmed by MRA or CTA; (3) No history of stroke or transient ischemic attack; (4) Good acoustic transmission of temporal window; (5) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Clinically confirmed non atherosclerosis related intracranial artery stenosis; 2.Diagnosed with neurodegenerative diseases such as Alzheimer's disease, Lewy body dementia, frontotemporal lobe degeneration, Parkinson's disease, and cognitive decline; 3.Severe neurological deficits prevent patients from living independently and are expected to be unable to complete follow-up plans; Or merge other diseases that may affect the judgment and follow-up of endpoint events, such as severe heart, lung, liver, kidney, endocrine diseases, etc; 4.Extracranial neck vascular stenosis>50%; 5.Relative/absolute contraindications related to the safety of magnetic resonance imaging (such as in vivo metal, claustrophobia, etc.); 6.Poor sound transmission through the temporal window; 7.Refusal to sign informed consent form.

Design outcomes

Primary

MeasureTime frame
Stroke;

Secondary

MeasureTime frame
Occurrence and progression of cognitive impairment;Myocardial infarction;Death (vascular and non-vascular), myocardial infarction, occurrence and progression of cognitive impairment, deterioration of functional status (mRS = 2 points);Deterioration of functional status (mRS >= 2 points);

Countries

China

Contacts

Public ContactXing Yingqi

Xuanwu Hospital Capital Medical University

xingyq2009@sina.com+86 10 83198966

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026