Actively Recruiting
MRI-Derived Pressure Ratio for Stroke Risk Assessment in Intracranial Atherosclerotic Stenosis
Led by Xuanwu Hospital, Beijing · Updated on 2025-12-30
400
Participants Needed
1
Research Sites
15 weeks
Total Duration
On this page
Sponsors
X
Xuanwu Hospital, Beijing
Lead Sponsor
X
Xuanwu Hebei Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying intracranial atherosclerotic stenosis (ICAS), a condition that increases the risk of stroke despite optimal medical treatments. This observational study aims to evaluate whether a new MRI-derived Pressure Ratio (MPR) can better predict stroke risk in patients with ICAS by measuring regional blood flow dynamics. The study is conducted across multiple stroke centers and is designed to improve risk assessment beyond current methods that focus mainly on the severity of artery narrowing. Participants will receive standardized medical therapy following AHA/ASA guidelines, including dual antiplatelet treatment and management of vascular risk factors. The study will use various imaging techniques such as transcranial Doppler, CT angiography, MR angiography, digital subtraction angiography, high-resolution MRI, and phase-contrast MR angiography to assess blood flow and calculate the MPR. Patients will be evaluated at baseline, and then at 1 month, 6 months, and 12 months after enrollment. During the study, participants will undergo multiple imaging assessments and clinical evaluations to monitor their condition and measure outcomes. The main outcome is the occurrence of ischemic stroke or related death in the affected artery territory within one year. Secondary outcomes include transient ischemic attacks, different types of strokes, and overall stroke or death risk within the same period. An independent Data and Safety Monitoring Board oversees the study's safety and conduct while participants remain under regular medical care throughout the 12-month follow-up.
CONDITIONS
Brief Title
MPR for Stroke Risk Assessment of ICAS
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 80 years
- Intracranial atherosclerotic stenosis involving a culprit artery in the anterior circulation
- Intracranial arterial stenosis of 50% to 99% measured by TCD, CTA, MRA, or DSA using the WASID method
- Written informed consent from the participant or legal representative
You will not qualify if you...
- Non-atherosclerotic intracranial lesions such as moyamoya disease, vasculitis, vascular dissection, autoimmune diseases, or congenital/genetic abnormalities
- More than 50% stenosis of the extracranial carotid artery on the same side
- Large cerebral infarction involving more than half the territory on imaging or a baseline modified Rankin Scale score of 3 or higher
- Contraindications to antiplatelet therapy or statins
- Inability to undergo MRI due to metal implants or claustrophobia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 12 months
Participants who undergo routine care are observed with multimodal imaging techniques and clinical assessments to evaluate stroke risk and vascular status over time.
Visits at baseline, 1 month, 6 months, and 12 months post-enrollment
Trial Site Locations
Total: 1 location
1
Department of Neurosurgery, Xuanwu hospital
Beijing, Xicheng District, China, 100053
Actively Recruiting
Research Team
J
Jichang Luo, M.D.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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