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 are generally well enough to carry out daily activities with little or no limitation (a standard measure of physical fitness used in cancer care must be 0 or 1)
- People with an expected survival of at least 3 months
- People who have been diagnosed with liver cancer (hepatocellular carcinoma) confirmed according to Chinese national liver cancer guidelines
- People whose cancer has not spread outside the liver, and whose cancer either cannot be removed by surgery or who have chosen not to have surgery
- People who have at least one clearly measurable tumour in the liver
- People whose tumours take up no more than 50% of the total liver volume
- People whose liver is functioning at an acceptable level (Child-Pugh score of 7 or below)
- People whose blood counts, liver function, kidney function, and blood clotting results all fall within the acceptable ranges required by the trial
- People of childbearing potential who agree to use effective contraception throughout the trial and for 6 months after it ends
Who may not be able to join:
- People who have previously had a condition where the liver stops filtering toxins properly, causing confusion or other brain symptoms (hepatic encephalopathy)
- People whose cancer has spread outside the liver, or who have another type of cancer
- People with a specific type of liver cancer that spreads through the liver tissue in a diffuse, infiltrating pattern rather than forming a distinct tumour
- People who have previously received any treatment for their liver cancer, including liver transplant, surgery, ablation, chemotherapy, radiation, targeted therapy, or immunotherapy
- People who have an abnormal structure in the liver's blood supply that would prevent certain procedures (TACE or SIRT) from being safely performed
- People who have a known allergy to contrast dyes or anaesthetic medications
- People with signs of serious complications related to liver disease, such as significant fluid build-up in the abdomen, severely swollen veins in the oesophagus or stomach, or advanced liver cirrhosis
- People with severely reduced lung function based on breathing test results
- People for whom the estimated radiation dose to a single lung would be too high (above 30 Gy)
- People who have a blood clot or tumour blocking major blood vessels connected to the liver, or blocking the bile duct
- People with a serious active infection that requires ongoing treatment
- People who are pregnant or breastfeeding
- People who test positive for HIV
- People with active hepatitis B virus (HBV) or hepatitis C virus (HCV) detected in the blood
- People with active syphilis or tuberculosis
- People who do not meet specific technical requirements on a pre-treatment imaging scan (a special nuclear medicine scan called 99mTc-MAA imaging), which checks whether the planned radiation treatment can be safely and effectively delivered (confirm with trial site for full technical details)
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
Principal Investigator: Gao-Jun Teng, Zhongda Hospital, Soueast University
Phone: +86-25-83272121
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
Time to progression (TTP)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.