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A Study on Intelligent Diagnostic and Therapeutic Evaluation for Malignant Tumors and Neurodegenerative Diseases Based on One-Day Dual-Tracer Whole-Body PET/CT Imaging

A Study on Intelligent Diagnostic and Therapeutic Evaluation for Malignant Tumors and Neurodegenerative Diseases Based on One-Day Dual-Tracer Whole-Body PET/CT Imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122442
Enrollment
Unknown
Registered
2026-04-14
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Pancreatic cancer, prostate cancer, Parkinson's syndrome, Alzheimers disease

Interventions

Patients initially suspected of or diagnosed with pancreatic cancer:None
Patients suspected of or diagnosed with prostate cancer for the first time:None
Patient suspected of PD at initial consultation:None
Patient suspected of AD at initial consultation:None
Healthy control group:None

Sponsors

Department of Nuclear Medicine, The First Medical Center of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. For patients with initially suspected or confirmed pancreatic cancer, whole-body PET/CT imaging with [68Ga]Ga-FAPI-04 plus [18F]FDG is required; for those with initially suspected or confirmed prostate cancer, whole-body PET/CT imaging with [68Ga]Ga-PSMA-11 plus [18F]FDG is indicated; or dual-molecular probe whole-body PET/CT imaging is necessary for suspected postoperative recurrence or metastasis to other sites. 2. Patients with Parkinson's disease (PD): meeting the International Parkinson and Movement Disorder Society diagnostic criteria for PD. Including: 1) bradykinesia; 2) at least one of muscular rigidity, resting tremor, or postural instability; 3) at least one of unilateral onset, persistent resting tremor, progressive course, predominantly asymmetrical involvement after onset, and a significant response to levodopa (70%-100%). 3. Patients with Alzheimer's disease (AD): according to the diagnostic criteria set by the American Alzheimer's Association in 2024. The diagnosis is supported by clinical cognitive assessment; cognitive impairment is mainly characterized by memory decline, without severe neuropsychiatric symptoms (such as aggression or severe agitation), and can cooperate with examinations with the assistance of a caregiver; without other central nervous system diseases (such as cerebrovascular disease, Lewy body dementia, cerebral amyloid angiopathy, etc.) to avoid confounding imaging result analysis. 4. Enrollment criteria for healthy control group include: 1) overall good health; 2) age and gender matched with the patient groups.

Exclusion criteria

Exclusion criteria: 1. Common exclusion criteria for PET use (e.g., implantable medical devices such as aneurysm clips, tattoos, claustrophobia, high fever, etc.); 2. Alcohol or drug dependence; 3. Major psychiatric disorders: including anxiety disorders, depression, affective disorders, schizophrenia, or drug-induced psychosis; 4. Neurological diseases: including cerebral infarction, brain tumors, cranial trauma, etc.; 5. Severe internal medical conditions, currently using respiratory drugs, cardiovascular drugs, anticonvulsants, or psychoactive substances; 6. Pregnant or lactating women and those planning pregnancy within one month during the trial; 7. Severe hearing and vision impairments; 8. Subjects unwilling to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
SUV value;

Countries

China

Contacts

Public ContactWang Ruimin

Department of Nuclear Medicine, The First Medical Center of PLA General Hospital

wrm@yeah.net+86 135 0115 1740

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026