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Evaluation of the association of 18F-AV45 PET / CT imaging and the clinical severity of Alzheimer's disease patients: a prospective, single-center clinical cohort study

Evaluation of the association of 18F-AV45 PET / CT imaging and the clinical severity of Alzheimer's disease patients: a prospective, single-center clinical cohort study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091472
Enrollment
Unknown
Registered
2024-10-29
Start date
2024-02-23
Completion date
Unknown
Last updated
2024-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's disease

Interventions

Exposed group:18F-SynVesT-1 PET / CT imaging

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 95 Years

Inclusion criteria

Inclusion criteria: Patients who visited the Department of Neurology of Peking University Shenzhen Hospital between October 2023 and September 2028 were included in this cohort . The inclusion criteria are: 1 The subject voluntarily or legal guardian agrees to participate in this trial and signed the informed consent. 2. Age 45 and 95 years old (subject to the date of signed informed consent), gender is not limited. 3. CU, MCI, and AD patients meeting the NIA-AA diagnostic criteria. 4 Expected survival time of more than 12 months. 5. Willing and able to comply with diagnostic plans, clinical laboratory tests, and other trial procedures.

Exclusion criteria

Exclusion criteria: Subjects will be excluded from this study if any of the following conditions exist: (1) the presence of neoplastic or significant cerebrovascular lesions; (2) neurosurgical or other neurological diseases, including epilepsy, encephalitis, or stroke; (3) clinically related mental illness; (4) current or recent history of drug or alcohol abuse / dependence. 2.There are thyroid dysfunction, vitamin B12 and folic acid deficiency, anemia, and neurosyphilis that may affect cognitive function. 3.Metabolic, immune, severe cardiac, liver, lung, renal disease, or tumors of any type were excluded. 4.Previous radionuclide administration and less than 10 physical half-lives apart from this study. 5.Is going or planning to participate in any drug or device clinical trial during the study. 6.Known allergy to the injection solution or its excipients. 7.Do not lie flat or remain still during the PET scan, or do not tolerate the PET scan. 8.Subjects with abnormalities in physical examination, ECG, EEG and clinical laboratory tests during the screening period that may affect safety or compliance.

Design outcomes

Primary

MeasureTime frame
clinical dementia rating;Standardized Uptake Value ratio;

Secondary

MeasureTime frame
asymmetry index;

Countries

China

Contacts

Public ContactMengjie Dong

PekingUniversityShenzhenHospital

dongmengjie@126.com+86 198 3286 1875

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026