Actively Recruiting

Age: 50Years +
All Genders
Healthy Volunteers
ID06477484

Blood-based Biomarkers for Early Alzheimer's Disease Screening

Led by Peking University First Hospital · Updated on 2024-06-27

180

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating blood biomarkers to improve early screening for Alzheimer's disease (AD). This observational study focuses on patients with AD, mild cognitive impairment (MCI) due to AD, and cognitively normal individuals. The goal is to identify key blood biomarkers suitable for early detection and to build a comprehensive model combining biomarkers and clinical information. The study is sponsored by Peking University First Hospital. Participants will have blood samples taken to test for specific biomarkers including Aβ40, Aβ42, P-Tau181, P-Tau217, GFAP, and NfL. These tests aim to evaluate their diagnostic accuracy for Alzheimer's and MCI. The study will observe individuals at different stages of cognitive health to understand how these biomarkers perform across groups. During the two-year study period, participants will undergo cognitive assessments and blood draws as part of the evaluation. Researchers will monitor the accuracy of these biomarkers in diagnosing AD and MCI. The study also aims to develop a model that combines blood biomarker results with clinical information to aid early identification. Participation involves regular assessments and cooperation with blood sampling and cognitive testing.

CONDITIONS

Brief Title

Blood Biomarkers for Screening of Alzheimer's Disease

Who Can Participate

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 65 50 years
  • Diagnosis of Alzheimer's disease according to 2011 NIA-AA criteria, mild cognitive impairment by 2004 Peterson criteria, or cognitively normal status
  • Signed informed consent form
Not Eligible

You will not qualify if you...

  • Presence of other disorders causing cognitive impairment
  • Unable to cooperate with cognitive assessments
  • Refusal to have blood drawn for testing

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 2 years

Participants undergo blood biomarker testing to evaluate markers associated with Alzheimer's disease.

Periodic blood draws over 2 years

Long-term Monitoring

Duration - Up to 2 years

Participants are monitored to assess the diagnostic accuracy of blood biomarkers combined with clinical information.

Follow-up assessments during the 2-year period

Trial Site Locations

Total: 1 location

1

Peking University First Hospital

Beijing, Beijing Municipality, China, 100034

Actively Recruiting

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Research Team

C

Chen Zhang

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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