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MPR for Stroke Risk Assessment of ICAS

MRI-Derived Pressure Ratio: a Novel Noninvasive Hemodynamic Biomarker for Stroke Risk Stratification in Intracranial Atherosclerotic Stenosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07309718
Enrollment
400
Registered
2025-12-30
Start date
2025-12-01
Completion date
2028-03-31
Last updated
2025-12-30

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

Conditions

Hemodynamic, ICAS - Intracranial Atherosclerosis, Stroke Ischemic

Keywords

ICAS - Intracranial Atherosclerosis, Stroke Ischemic, Hemodynamic, Pressure ratio

Brief summary

Intracranial atherosclerotic stenosis (ICAS) carries substantial stroke risk despite optimal medical treatment. Current risk stratification relies primarily on stenosis severity, but novel hemodynamic markers may improve prediction. In this multiple prospective registry study we aim to investigate whether regional hemodynamics, measured by a novel Magnetic resonance imaging-derived Pressure Ratio (MPR) technique, are associated with stroke risk in ICAS.

Detailed description

This study is a multicentre prospective single-arm registry study and the protocol is approved by the ethics committee at the coordinating centre and by the local institutional review board at each participating centre. This study is initiated by the investigators, with 5 participating stroke centres , and plans to recruit 400 consecutive patients who meet the inclusion and exclusion criteria. After the enrolment, all participants would be evaluated at baseline, 1 month, 6 months, and 12 months post-enrollment. All participants received standardized medical therapy, including dual antiplatelet treatment and management of vascular risk factors, in accordance with AHA/ASA guidelines. Multimodal imaging techniques were employed to assess hemodynamic status: luminal stenosis would be evaluated using transcranial Doppler (TCD), computed tomography angiography (CTA), magnetic resonance angiography (MRA), or digital subtraction angiography (DSA), high-resolution MRI and phase-contrast MR angiography (PC-MRA) would be collected to calculate MPR. The primary outcomes were ischemic stroke in the qualifying artery territory or related death within 1 year. There were 5 secondary outcomes, including hemodynamic ischemic stroke in the qualifying artery territory within1 year. An independent Data and Safety Monitoring Board (DSMB) oversees the conduction, safety and efficacy of the study.

Interventions

Dual antiplatelet treatment and management of vascular risk factors, in accordance with AHA/ASA guidelines

Sponsors

Xuanwu Hebei Hospital
CollaboratorUNKNOWN
Xuanwu Xiongan Hospital
CollaboratorUNKNOWN
Xuanwu Chifeng Hospital
CollaboratorUNKNOWN
Xuanwu Jinan Hospital
CollaboratorUNKNOWN
Xuanwu Hospital, Beijing
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Adults aged 18 to 80 years. 2. Intracranial atherosclerotic stenosis ICAS involving a culprit artery in the anterior circulation. 3. Intracranial arterial stenosis of 50% to 99% as measured by the WASID method using TCD, CTA, MRA, or DSA. 4. Written informed consent obtained from the participant or a legal representative.

Exclusion criteria

1. Non-atherosclerotic intracranial lesions, including moyamoya disease, vasculitis, vascular dissection, autoimmune diseases, or congenital/genetic abnormalities. 2. More than 50% stenosis of the extracranial carotid artery on the ipsilateral side. 3. Large cerebral infarction involving more than one-half of the territory on DWI imaging, or a baseline modified Rankin Scale score ≥3. 4. Contraindications to antiplatelet therapy or statins. 5. Inability to undergo MRI due to metal implants or claustrophobia.

Design outcomes

Primary

MeasureTime frameDescription
ischemic stroke in the qualifying artery territory or related death within 1 year after enrollment.12 monthsthe number of participants who suffer from ischemic stroke in the qualifying artery territory or related death within 1 year after enrollment.

Secondary

MeasureTime frameDescription
transient ischemic attack (TIA) or ischemic stroke in the qualifying artery territory within 1 year12 monthsthe number of participants who suffer from transient ischemic attack (TIA) or ischemic stroke in the qualifying artery territory within 1 year after enrollment.
TIA related to ischemia in the qualifying artery territory within 1 year12 monthsthe number of participants who suffer from TIA related to ischemia in the qualifying artery territory within 1 year
any stroke/TIA/ death within 1 year12 monthsthe number of participants who suffer from any stroke/TIA/ death within 1 year
hemodynamic ischemic stroke in the qualifying artery territory within 1 year12 monthsthe number of participants who suffer from hemodynamic ischemic stroke in the qualifying artery territory within 1 year
embolic stroke within in the qualifying artery territory 1 year12 monthsthe number of participants who suffer from embolic stroke within in the qualifying artery territory 1 year

Countries

China

Contacts

Primary ContactJichang Luo, M.D.
luojichang_dr@sina.com+86 13120136577

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026