Ireland
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Recruiting Not applicable

GPC3 Targeted Fluorescence Image Guided Surgery of Hepatocellular Carcinoma

NCT05047510 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2021-09-10
Last updated
2023-08-30

Condition(s) studied

Hepatocellular Carcinoma

Investigational drug(s) / intervention(s)

Anti-GPC3-IRDye800CW

Anti-GPC3-IRDye800CW: Drug Injection: Anti-GPC3-IRDye800CW

Study summary

This study is to evaluate whether intraoperative fluorescence imaging targeting GPC3 can aid improve the surgical accuracy of hepatocellular carcinoma.

The main purposes of this study include:

① To raise the detection rate of hepatocellular carcinoma intraoperatively using the novel NIR-II fluorescence molecular imaging and the GPC-3 targeted fluorophore.

② To validate the safety and effectiveness of the designed GPC-3 targeted fluorophore for clinical application.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Patients who have been diagnosed with hepatocellular carcinoma. 2. Planned to receive hepatectomy. 3. Liver function Child-Pugh A/B. 4. GPC-3 was validated highly expressed preoperatively. 5. Aged 18 to 75, and the expected lifetime is longer than 6 months. 6. Approved to sign the informed consent. Exclusion Criteria: 1. Allergic to IRDye800. 2. Enrolled in other trials in the past 3 months. 3. Another malignant tumor was found. 4. Undesirable function of heart, lung, kidney, or any other organs. 5. Unable to tolerate a hepatectomy. 6. The researchers considered inappropriate to be included.

Primary outcome measure(s)

  • HCC lesions — During hepatocellular resection surgery.
    Numbers of intraoperatively detected hepatocellular carcinoma lesions.

Trial sites (2)

FacilityCityRegionStatus
Zhuhai People's Hospital Zhuhai Guangdong Recruiting
The Affiliated Hospital of Southwest Medical University Luzhou Sichuan Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05047510 on ClinicalTrials.gov ↗ ← All trials in China