RecruitingNCT06402370

Amyloid PET in Patients With Mild Cognitive Impairment and Early Dementia


Sponsor

University Hospital, Ghent

Enrollment

50 participants

Start Date

May 8, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

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 defined using cerebrospinal fluid analysis but also non-invasively using an amyloid or tau PET scan. The N status can be defined using an \[18F\]-FDG PET scan which is in Belgium part of standard of care. Recently, it has been demonstrated, using different amyloid PET tracers, that early-frame amyloid scans can be a surrogate for \[18F\]-FDG PET scan.


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • Patients with mild cognitive impairment or early stage dementia who have a MRI and \[18F\]FDG PET/CT scan as part of routine clinical work-up

Exclusion Criteria1

  • Patient is not able to understand the study Patient is not able to lie still in the scanner for at least 30 minutes Pregnancy or breastfeeding

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DIAGNOSTIC_TESTPET scan

\[18F\]Vizamyl


Locations(1)

Van Weehaeghe D

Ghent, Belgium

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06402370


Related Trials