Multimodal Ophthalmic Imaging and Plasma Biomarkers for the Early Detection of Alzheimer's Disease

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50+
SponsorPeking University First Hospital

About this trial

With the accelerating global aging population, dementia has become a pressing worldwide issue. This project aims to identify specific plasma biomarkers and ocular indicators for the early detection of Alzheimer's disease (AD).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female participants aged ≥ 50 years;

Participants diagnosed with Alzheimer's Disease (AD), mild cognitive decline (MCI), subjective cognitive decline (SCD), or cognitively normal (CN);

Signed informed consent form

Disqualifiers

Presence of other neurological disorders and systemic diseases that may cause cognitive impairment;

Inability to cooperate with cognitive assessments;

Refusal to undergo blood sampling.

Trial population

AD, MCI, SCD and CN

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

  • Multimodal Ophthalmic Imaging and plasma biomarker

    Diagnostic test

    Multimodal Ophthalmic Imaging and plasma biomarkers (Aβ42/40, p-tau181, p-tau217, NfL and GFAP).

Treatment groups

200 Participants
are divided into 1 treatment group
Group A: Different stages of Alzheimer's disease1 intervention

Trial outcomes

Primary outcomes

1

Quantitative differences of core multimodal ophthalmic imaging parameters (including structural and functional ocular imaging indices) across study groups

Time frame
Baseline

Secondary outcomes

1

Concentration difference of plasma biomarkers (Aβ42/40, p - tau181, p - tau217, NfL and GFAP) among groups

Time frame
Baseline

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.