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Simple blood test could spot Alzheimer's early

NCT ID NCT07307872

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a new blood test that uses a microfluidic chip to detect Alzheimer's disease. Researchers collected blood and urine samples from 150 people, including those with Alzheimer's, other brain diseases, and healthy volunteers. The goal was to see if the test could accurately identify Alzheimer's by measuring specific biomarkers in red blood cells.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to a simple, non-invasive blood test for early Alzheimer's diagnosis, helping with patient care and clinical trial enrollment.
What could go wrong
This is an early-stage, non-interventional study. The test may not be accurate enough for widespread use, and results need validation in larger, more diverse populations.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

150 people

The number who actually took part.

Started

Mar 2017

Finished

Dec 2018

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population consists of 150 adults aged 50 to 85 years recruited at the Leenaards Memory Center (CHUV, Lausanne, Switzerland). Participants are divided equally into three groups: * Alzheimer's disease (AD) group: 50 patients diagnosed with Alzheimer's disease according to clinical, neuropsychological, neuroimaging, and CSF biomarker criteria. * Non-Alzheimer neurodegenerative disease (NAD) group: 50 patients with frontotemporal dementia (FTD) or Parkinson's disease (PD) responsive to L-DOPA, negative for AD biomarkers. * Healthy control (HC) group: 50 cognitively normal individuals with normal MRI and neuropsychological profiles. Participants are recruited during routine clinical evaluations or follow-up visits. Healthy controls are recruited through local advertisement within the hospital network. All subjects (or their legal representatives) provide written informed consent prior to participation.

Ages

50 to 85 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: General (all groups): * Male or female participants aged 50 to 85 years. * Signed and dated written informed consent (or consent from a legally authorized representative when applicable). Alzheimer's Disease (AD) Group: * Clinical diagnosis of Alzheimer's disease with a gradual and progressive decline in memory over at least 6 months. * Objective evidence of an amnestic syndrome of the hippocampal type (based on RLRI-16, MoCA, or equivalent tests). * Montreal Cognitive Assessment (MoCA) score between 15 and 23 (inclusive). * Structural MRI compatible with a typical AD diagnosis (3D volumetric MRI required; amyloid PET if available). * Retrospective CSF biomarker results showing at least 2 of 3 markers positive (Aβ1-42, total Tau, phosphorylated Tau). * Patients with familial AD forms (mutations in APP, PSEN1, or PSEN2) may also be included. Non-Alzheimer Neurodegenerative Disease (NAD) Group: * 25 patients with frontotemporal dementia (FTD) and 25 patients with Parkinson's disease (PD) responsive to L-DOPA. * Retrospective CSF biomarker results showing negative or non-AD profiles (≥2 of 3 markers negative). * Neuroimaging compatible with respective diagnoses: FTD: medial temporal atrophy and frontal atrophy score ≥2; MoCA 15-23. PD: evidence of dopaminergic neuron loss in substantia nigra; MoCA \>23. Healthy Control (HC) Group: * Normal cognitive status (MoCA \>23 and normal performance on RLRI-16 or equivalent neuropsychological tests). * Normal structural MRI (and normal PET scan, if available). * Negative CSF biomarkers (if available). Exclusion Criteria: General (all groups): * Neutropenia (neutrophils \<1,500/mm³) or thrombocytopenia (platelets \<100,000/mm³). * Education level below primary school. * History of psychiatric disorders (schizophrenia, psychosis). * Vascular dementia or mixed dementia. * Active infectious or chronic inflammatory diseases affecting blood cell function. * Active cancer or cancer under treatment, or treatment stopped within the last 3 months. * Use of medications interfering with cognitive function or biomarkers of interest. * Major sensory deficits (visual or auditory) affecting cognitive testing. * Epilepsy. * Known contraindication to MRI (e.g., stent or metallic implant). Group-specific exclusions: * AD group: Exclude vascular dementia, Lewy body dementia, mixed dementia, or any non-AD neurodegenerative disease. * NAD group: Exclude Alzheimer's disease, vascular, or mixed dementia. * HC group: Exclude any neurodegenerative disease, cognitive disorder, or abnormal cognitive testing.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Leenaards Memory Center - CHUV

    Lausanne, 1011, Switzerland

More trials for these conditions

Other studies related to the condition(s) this trial covers.