Amyloid PET in Patients With Mild Cognitive Impairment and Early Dementia
NCT ID: NCT06402370
Last Updated: 2024-05-20
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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RECRUITING
50 participants
OBSERVATIONAL
2024-05-08
2026-05-31
Brief Summary
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Detailed Description
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The National Institute on Aging together with the Alzheimer's Association (NIA-AA) recently proposed the ATN classification which is based upon the pathological processes present in Alzheimer's disease (amyloid, tau and neurodegeneration). The amyloid and tau status can be obtained using cerebrospinal fluid analysis but also non-invasively using an amyloid or tau PET scan. The N status can be obtained using an \[18F\]FDG PET scan which is in Belgium part of standard of care. Both the \[18F\]FDG PET scan and the amyloid scans using \[18F\]Vizamyl are also proposed in the diagnostic algorithm for early and differential diagnoses of dementia .
Perfusion scans using \[15O\]H2O have shown a good correlation with \[18F\]FDG PET, illustrating the potential of perfusion as a proxy for neuronal dysfunction. Previously, it has been demonstrated that early amyloid scans represent perfusion and can therefore be used as a proxy for neuronal activity.
Next generation PET/CT scanners, such as the Omni Legend have a very high sensitivity which may enable ultra-short PET scans, which is important is this vulnerable patient group, or dynamic scans with a high effective time resolution due to the possibility to acquire short time frames with reasonable noise characteristics. Moreover, the ultrashort scan may limit the movement artefacts frequently encountered in this study population.
The investigators hypothesize that a one minute scan 5 minutes postinjection is sufficient to determine the N-status of a patients and that a one minute scan 90-110 minutes postinjection can determine the A-status.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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PET scan
\[18F\]Vizamyl
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital, Ghent
OTHER
Responsible Party
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Principal Investigators
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Donatienne Van Weehaeghe, MD PhD
Role: PRINCIPAL_INVESTIGATOR
UZ Gent
Locations
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Van Weehaeghe D
Ghent, , Belgium
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ONZ-2023-0444
Identifier Type: -
Identifier Source: org_study_id
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