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Al18F-NOTA-FAPI-04 PET/CT for the diagnosis of malignant tumor

Al18F-NOTA-FAPI-04 PET/CT for the diagnosis of malignant tumor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096566
Enrollment
Unknown
Registered
2025-01-26
Start date
2025-02-08
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

malignancy

Interventions

Sponsors

Sichuan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Voluntary trial, with the patient or their legal representative signing an informed consent form; 2. Patient selection: Select patients who have been clinically diagnosed or diagnosed with malignant tumors in our hospital since November 22, 2023, and have complete clinical and follow-up data; 3. The criteria for diagnosing all subjects as malignant tumor patients are based on medical history, clinical manifestations, other imaging examinations such as X-rays, CT, MRI, and 18F-FDG PET-CT, and follow-up for more than 6 months.

Exclusion criteria

Exclusion criteria: 1. Individuals with a history of allergies to similar drugs (drugs with similar chemical or biological components to fibroblast activation protein inhibitors), allergic constitution, or current allergic diseases. 2. Those who are currently undergoing clinical trials of other drugs or have participated in clinical trials of any drugs (excluding vitamins and minerals). 3. There are other clinical problems that are difficult to control (such as HIV, hepatitis C virus infection or active hepatitis B, or other serious chronic infections and serious mental, neurological, cardiovascular, respiratory and other system diseases). 4. Pregnant and lactating women (where pregnancy is defined as a positive urine pregnancy test). 5. Patients whose physical condition is not suitable for radiation examination. 6. Researchers believe that exclusion is necessary.

Design outcomes

Primary

MeasureTime frame
Maximum standard uptake value ;mean standard uptake value ;

Secondary

MeasureTime frame
Tumor metabolic volume ;sensitivity;accuracy;specificity;

Countries

China

Contacts

Public ContactZhuzhong Cheng

Sichuan Cancer Hospital

chengzhuzhong@163.com+86 152 2888 0392

Outcome results

None listed

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