NCT06534658 · RECRUITING

Study on Multimodal Imaging and Molecular Imaging Techniques in Degenerative Dementia

This observational study is tracking people with Alzheimer's disease or mild cognitive impairment over time using brain scans, molecular imaging, blood markers, and digital tools. The goal is to better understand how these diseases progress and to find new ways to diagnose and monitor them. There is no drug or treatment being tested — researchers are collecting data only. The phase is unspecified, which is typical for observational studies.

You may qualify if

  • Patients aged ≥50 and ≤85 years old, male or female;
  • Meet the diagnostic criteria for dementia or MCI;
  • Neuropsychological score: MMSE 15-28 points, CDR ≤ 1 point; ④ Patients and their families are informed and sign the informed consent form

You're excluded if

  • The presence of other neurological diseases that may cause brain dysfunction (such as depression, brain tumors, Parkinson's disease, metabolic encephalopathy, encephalitis, multiple sclerosis, epilepsy, brain trauma, normal intracranial pressure hydrocephalus, etc.);
  • The presence of other systemic diseases that may cause cognitive impairment (such as liver dysfunction, renal dysfunction, thyroid dysfunction, severe anemia, folic acid or vitamin B12 deficiency, syphilis, HIV infection, alcohol and drug abuse, etc.);
  • Suffering from a disease that makes it impossible to cooperate with cognitive examinations;
  • The presence of contraindications to MRI;
  • The presence of mental and neurological retardation;
  • Refusing to draw blood;
  • Refusing to sign the informed consent form.

The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.

Eligibility criteria as of 2024-08-02

View full record on ClinicalTrials.gov

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