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Development and Clinical Trial of Molecular Probes for immunoPET Imaging of Digestive System Tumors

Development and Clinical Trial of Molecular Probes for immunoPET Imaging of Digestive System Tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200057692
Enrollment
Unknown
Registered
2022-03-15
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-11-06

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

Conditions

gastric cancer, liver cancer, pancreatic cancer

Interventions

Index test:PET/CT examination.

Sponsors

Department of Nuclear Medicine, Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. a. Those who are pathologically diagnosed as primary gastric adenocarcinoma and plan to perform PET/CT imaging; b. Pathologically diagnosed as a primary neuroendocrine tumor of the pancreas and proposed PET/CT imaging; c. Those who are pathologically diagnosed as primary malignant tumor of liver and plan to perform PET/CT imaging. 2. Tumor diagnostic criteria: The diagnosis and classification of liver cancer, gastric cancer and pancreatic cancer shall be carried out according to the 2019 WHO classification criteria for digestive tract tumors; 3. Do not take or inject drugs that interfere with imaging of relevant radionuclide labeled probe within 3 days before PET/CT examination; 4. Obtain/sign the informed consent form; 5. Did not participate in other clinical trials.

Exclusion criteria

Exclusion criteria: 1. Complicated with serious systemic diseases, such as systemic infection, cardiac insufficiency, liver and kidney insufficiency, blood disease, thyroid disease, autoimmune disease, etc; 2. Patients with tumors other than liver cancer, gastric cancer or pancreatic cancer; 3. Mental disorders or failure to cooperate due to poor compliance of mental retardation; 4. Pregnant and lactating women; 5. Have a history of surgery and trauma that significantly affect the metabolic distribution and anatomical structure; 6. Other situations judged by the researcher to be unsuitable for this experiment.

Design outcomes

Primary

MeasureTime frame
Maximum standard uptake value;

Countries

China

Contacts

Public ContactCheng Dengfeng

Department of Nuclear Medicine, Zhongshan Hospital, Fudan University

cheng.dengfeng@zs-hospital.sh.cn+86 13681927549

Outcome results

None listed

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