Clinical trial Recruiting at 1 site Observational

Study of biomarkers in liver cancer after surgery

Official title: Biomarkers and Molecular Mechanism Study of Hepatocellular Carcinoma After Radical Resection and Conversion Therapy

Run by Shanghai Zhongshan Hospital · NCT06382103 · Data updated 2026-11-12

This study looks at blood samples from liver cancer patients who had surgery to see if certain markers can help predict their long-term health and guide their treatment.

More Hepatocellular Carcinoma trials

Quick facts

Study typeObservational
SexAll
Enrollment240 (estimated)
SponsorShanghai Zhongshan Hospital
Academic / other
Locations1 site (Shanghai)
StatusRecruiting
StartedMay 15, 2024
Main results expectedMay 20, 2025
Study endsMay 20, 2026
Registry record updatedMarch 26, 2025
Trial IDNCT06382103 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients with a first diagnosis of hepatocellular carcinoma who are scheduled for surgical treatment.

Probably not a fit

Patients with secondary liver cancer, intrahepatic cholangiocarcinoma, or other concurrent malignancies may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to analyze blood samples from patients with hepatocellular carcinoma (HCC) who have undergone surgical resection. It focuses on identifying circulating tumor DNA (ctDNA) and plasma protein levels to enhance the prediction of long-term prognosis and inform treatment options. By monitoring ctDNA and conducting plasma proteomic analysis, the study seeks to improve patient outcomes following surgery. The findings could lead to more personalized treatment strategies for HCC patients.

Why it matters

Potential benefit: If successful, this study could provide more accurate prognostic information and tailored treatment options for patients with hepatocellular carcinoma.

How similar studies have gone: Other studies have shown promise in using ctDNA and plasma proteomics for cancer prognosis, indicating a potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with a first diagnosis of HCC.
* Patients with HCC who are to undergo surgical treatment, with or without neoadjuvant therapy.
* Ability to obtain tissue sample for ctDNA analysis and detectable baseline ctDNA level.

Exclusion Criteria:

* Patients with secondary liver cancer, or intrahepatic cholangiocarcinoma.
* Any other concurrent malignancy.
* History of organ transplant or hepatic encephalopathy.

Where it's running

  • Zhongshan Hospital Fudan University
    Shanghai, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.