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Preliminary evaluation of clinical application of SPECT imaging targeting GPC3

To explore the clinical value of SPECT imaging targeting GPC3 in hepatocellular carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103505
Enrollment
Unknown
Registered
2025-05-30
Start date
2025-06-10
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Patients with clinically highly suspected or histopathology hepatocellular carcinoma

Interventions

Gold Standard:The final diagnostic criteria were histopathology biopsy or surgical specimen, or a definite clinical diagnosis
Index test:SPECT imaging

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.the subject or his/her legal representative can sign and date the informed consent form; 2.commitment to follow the research procedures and cooperate in the implementation of the full-process research; 3.patients with high clinical suspicion or histopathology diagnosis of HCC and generally in good condition; 4.patients with a history of hepatocellular carcinoma who recur after treatment; 5.women in their reproductive years were using contraception for at least one month before screening and were committed to using contraception throughout the study period and for the prescribed period after the end of the study;

Exclusion criteria

Exclusion criteria: 1.inability to complete SPECTCT examination (including inability to lie down, claustrophobia, radiophobia, etc.); 2.acute systemic diseases and electrolyte disorders; 3.patients with known hypersensitivity to GPC3 imaging agents or synthetic excipients; 4.patients considered by the investigator to have poor adherence; 5.pregnant or lactating patients; 6.Have other factors not suitable to participate in this test;

Design outcomes

Primary

MeasureTime frame
Radiation dose to human body;Region of Interest,ROI;

Secondary

MeasureTime frame
Pathological results of tumour tissue;Radioactivity in the blood and urine samples;

Countries

China

Contacts

Public ContactXiaoli Lan

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

hzslxl@163.com+86 27 8572 6685

Outcome results

None listed

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