New scan may reveal hidden Alzheimer's in stroke survivors
NCT ID NCT02813434
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a special PET scan using florbetapir can help doctors figure out why some people develop memory and thinking problems after a stroke. The scan looks for amyloid plaques, a hallmark of Alzheimer's disease. Researchers studied 92 adults aged 40 to 80 who had a stroke and later experienced cognitive issues. The goal was to see how often Alzheimer's might be the underlying cause, which could guide better diagnosis and care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- florbetapir (a radioactive tracer for PET scans)
- What this could lead to
- If successful, this could help doctors better identify whether Alzheimer's disease is causing cognitive decline after a stroke, leading to more targeted care.
- What could go wrong
- This is a completed Phase 3 study with 92 participants, so results are available but may not apply to all stroke survivors. The scan is for diagnosis only, not treatment.
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.
- Phase
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
92 people
The number who actually took part.
- Started
-
Sep 2014
- Finished
-
Jan 2025
- Lead sponsor
-
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.
- Ages
-
40 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
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: 1. patients suffering of parenchymal stroke visualized by imaging (MRI), 2. patients suffering from cognitive impairment on the 6 months assessment (including GRECogVASC patients), 3. age between 40 and 80 years, 4. French-speaking, 5. reliable informant, 6. agreeing to participate in the study, 7. affiliation to a social security system, Exclusion Criteria: 1. women of childbearing potential (defined as pre-menopausal, less than 2 years postmenopausal, or not surgically sterile), or who are breast-feeding 2. history of relevant severe drug allergy or hypersensitivity, 3. patient receiving any investigational medications at least in the 30 last days, 4. stroke affecting the cerebellum, 5. mental retardation, 6. illiteracy, 7. dementia diagnosed before stroke, 8. history of schizophrenia or psychiatric illness requiring a stay for \> 2 days in a psychiatry unit, 9. persons placed under judicial protection, 10. comorbidities affecting cognition (respiratory, renal, liver, heart failure), 11. persistent disturbance of consciousness defined by a score to item 1a of the National Institute of Health Stroke Scale (NIHSS) ≤ 1, 12. contraindication to MRI.
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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.
Contacts and locations
Locations
-
CHU Amiens
Amiens, 80054, France
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