ConditionAlzheimer's Disease (AD)
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age55-85
SponsorUniversitaire Ziekenhuizen KU Leuven
About this trial
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.
Eligibility criteria
Qualifiers
Patients between 55 and 85 years old who consult their PCP due to concerns about their cognitive status.
Disqualifiers
Comorbidities that would interfere with study cooperation or interpretability of study results (for instance substance abuse or cardiac, renal or hepatic failure).
Concomitant medications that would interfere with cognitive assessments.
A prior diagnosis of AD and related disorders or other neurodegenerative disease.
Trial design
Treatments tested in this trial
- ptau217
Treatment groups
240 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov