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Development of an Integrated Nano-Molecular Imaging Theranostic Platform and Its Application in Urological Tumors

Development of an Integrated Nano-Molecular Imaging Theranostic Platform and Its Application in Urological Tumors

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121454
Enrollment
Unknown
Registered
2026-03-31
Start date
2025-01-08
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Tumors related to the kidney, bladder, and prostate gland

Interventions

Experimental group(Prostate cancer, Bladder cancer, Kidney cancer):Treated with the Nano-Molecular Imaging Diagnosis and Therapy Integrated Platform
Control group(Prostate cancer, Bladder cancer, Kidney cancer):Treated with conventional therapy (without using the Nano-Molecular Imaging Diagnosis and Therapy Integrated Platform)

Sponsors

Harbin Medical University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age over 18 years old, gender not restricted; 2. Patients diagnosed with prostate cancer, bladder cancer or kidney cancer; 3. Patients who have undergone PET/CT examination; 4. Patients subsequently confirmed by pathological examination; 5. Patients receiving therapeutic radionuclide combined with immunotherapy; 6. Patients who agree to use their medical records and examination results for research; 7. Patients whose important medical records or examination results were previously missing but have been corrected.

Exclusion criteria

Exclusion criteria: 1. Patients who have recovered from major trauma (including surgery) within 4 weeks prior to receiving medical technology treatment; 2. Patients with severe systemic or local infections or other serious coexisting diseases; 3. Patients with abnormal immune function or who have recently used immunosuppressants, enhancers (including various vaccines), etc.; 4. Patients with autoimmune diseases, including rheumatoid arthritis, etc.; 5. Patients with poorly controlled arrhythmias, including atrial fibrillation; 6. Patients with cardiac insufficiency (NYHA standard II) in New York; 7. Patients with uncontrolled hypertension; 8. Patients with any history of allergy to the components of the imaging agent, including antibodies, or with allergic constitution; 9. Subjects positive for syphilis, HBV, HCV, and HIV; 10. Male and female subjects of childbearing age who cannot take effective contraceptive measures; 11. Pregnant or lactating women; 12. Patients with mental illness or related medical history; 13. Patients who cannot or are unable to undergo PET/CT scans; 14. Other patients that medical technicians consider not meeting the requirements for the relevant type of disease.

Design outcomes

Primary

MeasureTime frame
Safety indicators;Efficacy indicators.;

Secondary

MeasureTime frame
Imaging indicators;Molecular imaging indicators;Survival outcome indicators;

Countries

China

Contacts

Public ContactKezheng Wang

Harbin Medical University Cancer Hospital

wangkezheng9954001@163.com+86 451 8571 8900

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026