A Prospective Cohort of Patients With Cervical/Intracranial Arteries Stenosis in China
NCT ID: NCT06595342
Last Updated: 2024-10-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
60000 participants
OBSERVATIONAL
2024-10-30
2030-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with cervical/intracranial arteries stenosis
Investigators plan to enroll 60000 patients with cervical/intracranial arteries stenosis including mild stenosis, moderate stenosis, severe stenosis or occlusion.
No intervention
no intervention
Interventions
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No intervention
no intervention
Eligibility Criteria
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Inclusion Criteria
2. Ultrasound or imaging examinations indicating cervical artery stenosis and/or intracranial artery stenosis (including mild, moderate, severe stenosis, or occlusion);
3. Willing to participate and signing the informed consent form.
Exclusion Criteria
2. Patients with severe systemic diseases, such as respiratory failure, renal failure, gastrointestinal bleeding, coagulation disorders, malignancies, etc.;
3. Patients with a life expectancy of less than one year or those who are unable to complete the study for other reasons.
40 Years
80 Years
ALL
No
Sponsors
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The First Hospital of Jilin University
OTHER
Responsible Party
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Yi Yang
The associate deam
Locations
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First Hospital of Jilin University
Changchun, Jilin, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ARTERIES
Identifier Type: -
Identifier Source: org_study_id
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