NCT06402370

Amyloid PET in Patients With Mild Cognitive Impairment and Early Dementia

University Hospital, Ghent·ClinicalTrials.gov·diagnostic testRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
MCI
Drug/Device/Intervention
PET scan
Study type
Observational
Intervention type
diagnostic test
Sponsor & location
Primary sponsor
University Hospital, Ghent
Location
Gent, Belgium
Timeline & enrollment
Phase
N/A
Start date
May 08, 2024
End date
May 01, 2026
Enrollment
50 participants
Primary outcome

N-status,A-status

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.

ICD-10 classifications
Microtia
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06402370
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06402370 through Pure Global AI's free database. This phase not specified trial is sponsored by University Hospital, Ghent and is currently Recruiting. The study focuses on MCI. Target enrollment is 50 participants.

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