Liver Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with liver cancer (HCC) that has not spread to the lymph nodes or other parts of the body.
- People who have previously had surgery or a radiofrequency ablation procedure to treat their liver cancer, with no signs of the cancer coming back within the first 6 months after that treatment.
- People whose liver cancer falls within specific size and spread limits: either one tumor smaller than 5 cm, or no more than three tumors each smaller than 3 cm, with no invasion into blood vessels and no spread outside the liver.
- People who have enough healthy liver tissue remaining outside the area being treated (more than 700 ml in volume).
- People who do not have serious problems with their blood, heart, lungs, liver, kidneys, or immune system.
- People whose blood test results meet the required levels for red blood cells, white blood cells, infection-fighting cells, and platelets (confirm with trial site for exact values).
- People who are able to have children and are willing to use contraception during the trial.
- People who are in a good general physical condition and have acceptable liver function, as measured by standard medical scoring tools (confirm with trial site).
- People who are expected to live for more than 3 months.
- People who are willing to take part voluntarily and sign a consent form.
Who may not be able to join:
- People who have already received anti-cancer treatment specifically for their liver cancer.
- People with significant liver scarring (cirrhosis), recent bleeding from the digestive tract related to liver pressure problems, or poor liver function scores.
- People whose liver function blood tests show certain levels are too high — specifically, bilirubin more than 1.5 times the normal upper limit, or two liver enzymes (ALT and AST) more than 2.5 times the normal upper limit, or a specific liver function test result of 40% or above (confirm with trial site).
- People who have had major surgery within one month before the study begins.
- People who have a history of another cancer, unless they had basal cell skin cancer or early-stage cervical cancer and have been cancer-free for more than 3 years after treatment.
- People who have taken part in another clinical trial within 30 days before this study's treatment begins.
- People whose tumor is located very close (less than 0.5 cm) to the stomach or intestines.
- People who are pregnant, breastfeeding, or able to have children but not willing to use contraception.
- People with a history of drug addiction, long-term heavy alcohol use, or HIV/AIDS.
- People with uncontrolled epileptic seizures or a mental illness that significantly affects their awareness or judgment.
- People with a history of severe allergic reactions or who are known to have unusual sensitivities (confirm with trial site).
- People whom the trial researchers consider unsuitable for participation for other reasons.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +86 0571 87783820
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Local control rate(LC)
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Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.