Under construction – not a live service
Sign in
Taking people in BelgiumNo phase

Blood tests for Alzheimer's disease in people with memory concerns seen by family doctors

Tests a blood marker, ptau217, for Alzheimer's disease in people with cognitive concerns.

Plain-language title generated from the registry record
Registry title: Blood-based Biomarkers for Alzheimer's Disease at the Primary Care Level.

Key facts

Where
Leuven, BelgiumSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 55 and 85 years old?

Source: NCT07666113, who can take part

Where in Belgium

  • UZ Leuven/KU LeuvenLeuven, BelgiumTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Universitaire Ziekenhuizen KU Leuven
Trial code
NCT07666113
Record updated
24 June 2026
Original description
The goal of this study is to determine how blood biomarker tests (ptau217 and ptau217/Aβ42) performed in primary care influence the patient trajectory in individuals with cognitive concerns.Read full original descriptionShow less

The Diagnostic Validity and Clinical Impact of Blood-based Biomarkers for the Diagnosis of Alzheimer's Disease at the Primary Care Level.

The goal of this study is to determine how blood biomarker tests (ptau217 and ptau217/Aβ42) performed in primary care influence the patient trajectory in individuals with cognitive concerns.

Participants will provide a blood sample for biomarker testing and undergo clinical assessments as part of diagnostic evaluation.

Inclusion: Patients between 55 and 85 years old who consult their PCP due to concerns about their cognitive status.

Exclusion: Concomitant medications that would interfere with cognitive assessments; A prior diagnosis of AD and related disorders or other neurodegenerative disease; Comorbidities that would interfere with study cooperation or interpretability of study results (for instance substance abuse or cardiac, renal or hepatic failure).

ClinicalTrials.gov NCT07666113