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Study of the Indications for Amyloid Positon Emission Tomography (PET) Scans and Their Usefulness for Patients With Suspected Alzheimer's Disease (AD) (TEPAmy)

C

Central Hospital, Nancy, France

Status

Completed

Conditions

Alzheimer Disease

Treatments

Other: Retrospective study

Study type

Observational

Funder types

Other

Identifiers

NCT06467981
2024PI105

Details and patient eligibility

About

The recent clinical authorization of amyloid Positon Emission Tomography (PET) in France represents a crucial step for the nuclear medicine community involved in the diagnosis of Alzheimer's disease (AD).

Full description

The recent clinical authorization of amyloid Positon Emission Tomography (PET) in France represents a crucial step for the nuclear medicine community involved in the diagnosis of Alzheimer's disease (AD). At the era of Amyloid, Tau, Neurodegeneration (ATN) biomarkers, amyloid PET fills a need in patients with an atypical or mixed clinical presentation, in particular young patients (< 65 years old), when the lumbar puncture is contraindicated or not feasible for technical reasons. Importantly, a negative amyloid PET scan discards the diagnosis of AD. Furthermore, early phase imaging of amyloid PET allows to estimate the perfusion neuronal state, increasing the diagnostic value of such PET radiotracer. Its role could be further developed in routine care for the selection and monitoring of promising disease modifiers therapies.

Enrollment

160 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged = or > 18 years
  • Patients who have had an amyloid PET scan with a PET request form including the indications for the examination
  • Patient informed via a newsletter and non-opposition to the use of their data for research purposes (research objectives clearly explained in the letters)

Exclusion criteria

  • Patient opposition to the use of their data for this research

Trial contacts and locations

1

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Central trial contact

Antoine VERGER, MD, PhD; Veronique ROCH, MSc

Data sourced from clinicaltrials.gov

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