Can brain scans predict the progression of silent stroke damage?
NCT ID NCT07726654
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
This observational study follows 400 adults with cerebral small vessel disease (CSVD) to understand how the condition progresses over time. Participants undergo annual brain scans (MRI and PET), cognitive tests, and blood work to track changes in brain structure, blood flow, and memory. The goal is to identify early markers of disease worsening, which could eventually help doctors intervene sooner.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could reveal early biomarkers and patterns of brain damage in cerebral small vessel disease, guiding future treatments.
- What could go wrong
- As an observational study, it does not test any treatment. Results may not lead directly to therapies, and findings may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 400 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The population consists of vascular dementia, vascular mild cognitive impairment, and cognitively normal participants.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥18 years. 2. Evidence of cerebral small vessel disease (CSVD) on brain MRI, meeting at least one of the following imaging criteria: * White matter hyperintensities (WMH) with a total Fazekas score ≥2; * Fazekas score =1 with at least two vascular risk factors (hypertension, hyperlipidemia, diabetes mellitus, obesity, current smoking, or a history of vascular events other than stroke); * Fazekas score =1 accompanied by the presence of lacunes; * Imaging evidence of a recent subcortical lacunar infarction. 3. Independent in activities of daily living (modified Rankin Scale \[mRS\] ≤2). 4. Able and willing to provide written informed consent. Exclusion Criteria: 1. Acute ischemic stroke with a diffusion-weighted imaging (DWI) lesion \>20 mm in diameter. 2. Acute intracerebral hemorrhage. 3. Acute subarachnoid hemorrhage, a history of aneurysmal subarachnoid hemorrhage or cerebrovascular malformation, or the presence of an untreated intracranial aneurysm \>3 mm in diameter. 4. Previously diagnosed neurodegenerative disorders, such as Alzheimer's disease (AD) or Parkinson's disease (PD). 5. Definite non-vascular white matter diseases, including multiple sclerosis, adult-onset leukodystrophy, metabolic encephalopathy, or other non-vascular white matter disorders. 6. Major psychiatric disorders diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5). 7. Contraindications to MRI (e.g., severe claustrophobia or MRI-incompatible implants). 8. Severe systemic diseases (e.g., active malignancy) with an expected life expectancy of less than 5 years. 9. Inability to complete scheduled follow-up because of geographic, logistical, or other reasons. 10. Concurrent participation in another interventional clinical trial.
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Ruijin Hospital affiliated to Shanghai Jiaotong University School of Medicine
Shanghai, Shanghai Municipality, 200025, China
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Other studies related to the condition(s) this trial covers.
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