Brain scan and blood test study aims to predict stroke recovery
NCT ID NCT07611136
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 180 adults with cerebral small vessel disease to see how their condition changes over time after a stroke. Researchers will use MRI scans and blood tests to track disease progression and look for links to thinking skills, daily function, and stroke recurrence. The goal is to better understand the disease and find new ways to monitor it.
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 help doctors better predict how small vessel disease progresses after a stroke, potentially guiding future treatments.
- What could go wrong
- This is an observational study, not a treatment trial, so it won't directly improve health. Results may not apply to all patients, and biomarkers may not reliably predict disease course.
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 180 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Apr 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
Adult patients with sporadic, non-genetic cerebral small vessel disease
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Age ≥ 18 years * Evidence of cerebral small vessel disease on brain MRI, defined as white matter hyperintensities (Fazekas grade 1-3) * Assignment to one of the following study groups based on MRI findings: * cerebral small vessel disease without evidence of an acute ischemic stroke * cerebral small vessel disease with acute lacunar ischemic stroke * cerebral small vessel disease with acute territorial ischemic stroke * Ability to provide written informed consent * Sufficient German language skills to understand study procedures and assessments Exclusion Criteria: * Alternative plausible causes of white matter hyperintensities other than cerebral small vessel disease (e.g. inflammatory central nervous system disorders, leukodystrophies, brain tumors) * Known neurodegenerative diseases (e.g. Parkinson's disease, Alzheimer's disease, other dementias) * Acute or recent traumatic brain injury * Contraindications to magnetic resonance imaging * Pregnancy or breastfeeding * Life expectancy of less than one year * Inability to comply with study procedures or follow-up visits
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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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University Hospital Ulm, Department of Neurology, Germany
RECRUITINGUlm, Baden-Wurttemberg, 89081, Germany
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