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Imaging study of brain blood vessel disease in adults

Builds a multi-center imaging cohort of people with cerebrovascular disease to study outcomes.

Plain-language title generated from the registry record
Registry title: Multi-Modality Imaging Standard Cohort Of Cerebrovascular Disease

Key facts

Where
Beijing, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT06925178, who can take part

Where in China

  • Beijing Tiantan HospitalBeijing, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Beijing Tiantan Hospital
Trial code
NCT06925178
Record updated
13 April 2025
Original description
The aim of this study is to establish a multi-center and multi-modality imaging standard cohort of cerebrovascular disease, analyze the potential mechanisms affecting the prognosis of cerebrovascular disease based on a variety of imaging methods, and explore potential therapeutic targets.Read full original descriptionShow less

Multi-Modality Imaging Standard Cohort Of Cerebrovascular Disease

The aim of this study is to establish a multi-center and multi-modality imaging standard cohort of cerebrovascular disease, analyze the potential mechanisms affecting the prognosis of cerebrovascular disease based on a variety of imaging methods, and explore potential therapeutic targets.

Inclusion: Age between 18 and 80 years old; Onset of symptoms within 7 days; Clinical diagnosis of cerebrovascular disease (ischemic stroke or hemorrhagic stroke) confirmed by head imaging (CT or MRI); Signed informed consent form.

Exclusion: Diagnosed with non-cerebrovascular diseases (such as central nervous system infections, epilepsy, and metabolic encephalopathy); Patients with contraindications to multimodal CT or MRI, functional near-infrared imaging, or those who cannot cooperate to complete the relevant examinations; Patients with a life expectancy of less than 3 months or those who cannot complete the study follow-up due to other reasons.

ClinicalTrials.gov NCT06925178