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Clinical Application Study of CCK2R PET/CT Tumor Imaging

Clinical Application Study of CCK2R PET/CT Tumor Imaging

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089478
Enrollment
Unknown
Registered
2024-09-09
Start date
2024-09-09
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

medullary thyroid carcinoma

Interventions

Sponsors

Fudan University Shanghai Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign the informed consent form. 2. Age = one year old. 3. MTC patients highly suspected or confirmed by pathological or routine imaging examinations, with CT levels>150 pg/mL and CEA greater than the upper limit of the reference value. According to the doctor's judgment, the expected survival period is 3 months. 5. Agree to implement strict contraception for at least 28 days after PET/CT examination. 6. Willing and able to follow the research plan.

Exclusion criteria

Exclusion criteria: If any of the following conditions exist in the subjects, they will be excluded from this study: Patients diagnosed with other malignant tumors in the past year. 2. Thyroid cancer patients diagnosed with other pathological types during follow-up. 3. Patients undergoing any anti-tumor treatment between two PET/CT scans. 4. Pregnant or lactating women. 5. Cannot lie down on the PET/CT scanning bed or tolerate PET examination during the scanning period. 6. Patients who have received or are currently receiving treatments such as radiotherapy, chemotherapy, immunotherapy, or molecular targeted therapy. 7. Have participated in other interventional clinical trials within the previous month before screening. 8. Patients who have been lost to follow-up. According to the researcher's assessment, the subjects have other circumstances that may affect the study or make them unsuitable to participate in the study.

Design outcomes

Primary

MeasureTime frame
SUVmax (Standardized Uptake Value max);

Countries

China

Contacts

Public ContactShaoli Song

Fudan University Shanghai Cancer Center

shaoli-song@163.com+86 138 1660 8573

Outcome results

None listed

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