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 volunteersQualifiers
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
Case-control
Cross-sectional
Treatments tested in this trial
Multimodal Ophthalmic Imaging and plasma biomarker
Diagnostic testMultimodal Ophthalmic Imaging and plasma biomarkers (Aβ42/40, p-tau181, p-tau217, NfL and GFAP).
Treatment groups
Trial outcomes
Primary outcomes
Quantitative differences of core multimodal ophthalmic imaging parameters (including structural and functional ocular imaging indices) across study groups
Secondary outcomes
Concentration difference of plasma biomarkers (Aβ42/40, p - tau181, p - tau217, NfL and GFAP) among groups
Sponsors and contacts
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