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NCT05187819

Blood-based Biomarkers for Diagnosis of Alzheimer's

Recruiting now NA Last updated 28 September 2023
What this trial tests

NA trial testing predictive value of a blood test in Dementia Alzheimers in 300 participants. Currently enrolling.

Timeline
1 June 2023
Primary endpoint
31 December 2026
31 December 2029

Quick facts

Lead sponsorHelse Stavanger HF
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposediagnostic
Enrollment300
Start date1 June 2023
Primary completion31 December 2026
Estimated completion31 December 2029
Sites1 location across Norway

Drugs / interventions tested

Conditions studied

Sponsor

Helse Stavanger HF — full company profile →

Who can join

Adults 40 to 100, any sex, with Dementia Alzheimers. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Alzheimer's disease (AD) may currently be diagnosed using molecular biomarkers in cerebrospinal fluid (CSF) and/or positron emission tomography (PET). These diagnostic procedures are highly accurate, but the high cost and low availability hamper their feasibility. Recently, ultrasensitive blood tests predicting Alzheimer pathologies in the brain have been developed. These tests have a reliable ability to differentiate AD from other neurodegenerative disorders and identify AD across the clinical continuum with high sensitivity and specificity in research cohorts with a high prevalence of AD. This project will assess the predictive value of these tests in a general practice population. The hypothesis is that the actual blood panel will have high positive predictive value for a diagnosis of Alzheimer's disease in the primary health care setting.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Dementia Alzheimers

Currently open trials in the same condition.

Other Helse Stavanger HF trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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