Three-in-One Stop Computed Topography Angiography(CTA) and CT Perfusion(CTP) in Cerebrovascular Disease
NCT ID: NCT06890468
Last Updated: 2025-03-24
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
1000 participants
OBSERVATIONAL
2025-03-16
2029-12-30
Brief Summary
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Detailed Description
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This study takes patients with cerebrovascular diseases as the research subjects and adopts a prospective cohort study design. The aim is to innovatively develop and verify a "one-stop" multimodal CT examination scheme. The 301-CTAP multimodal CT technology means that the three modalities are obtained through a single acquisition, including head and neck CTA (CTA), multiphase CTA (CTA) imaging of the brain, and CT perfusion imaging of the brain. The 301-CTAP multimodal CT technology can reduce the duration of CT examination for patients with cerebrovascular diseases without reducing the imaging content, and reduce the amount of contrast agents, X-ray radiation dose, and the incidence of contrast agent allergy and related adverse events. It provides innovative and important technical support for the diagnosis and assessment of acute stroke and other cerebrovascular emergencies; the acquisition of multiple key imaging indicators features enables individualized comprehensive imaging assessment, prediction of clinical functional prognosis and stroke recurrence risk for patients; the implementation of this project helps optimize the imaging examination path in the diagnosis and treatment of cerebrovascular diseases.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Head and neck artery stenosis/occlusion, moyamoya disease, aneurysm, artery dissection, etc., may include patients with acute stroke, chronic cerebral ischemia, and asymptomatic patients. After clinical assessment, CT perfusion imaging is required
* The image quality meets the requirements of diagnosis and post-processing
* Patients who follow the scanning strategy to complete the examination
* The patient or his or her family agrees to provide clinical data and follow-up
* Patients or their families sign informed consent forms
Exclusion Criteria
* People who are allergic to iodine contrast agents, or who cannot be tested temporarily due to taking metformin or aminoglycoside drugs
* Renal failure patient
* Severe cardiac insufficiency
* Severe liver damage
* Patients with an expected survival of less than 1 year
* Patients with cerebrovascular diseasePregnant woman
18 Years
100 Years
ALL
No
Sponsors
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Xin Lou
OTHER
Responsible Party
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Xin Lou
Chairman
Principal Investigators
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Xin Lou
Role: STUDY_CHAIR
Chinese PLA General Hospital
Locations
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Chinese PLA General Hospital, Beijing, Beijing 100853
Beijing, , China
Countries
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Central Contacts
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Other Identifiers
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301-CTAP
Identifier Type: -
Identifier Source: org_study_id
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