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 aged 18 to 75 years old who have liver cancer or other liver tumours and are scheduled for a keyhole (laparoscopic) liver removal surgery that targets a specific section of the liver
- People whose liver is functioning at a level rated as Grade A or B on a standard medical scoring system called Child-Pugh
- People who have no medical reasons preventing them from having keyhole liver surgery
- People whose life expectancy is at least 3 months
- People who are generally well enough to carry out light activity, rated 0 or 1 on a standard health performance scale (ECOG PS)
- People whose major organs are working well and whose recent blood test results (taken within 7 days before joining) meet specific minimum levels for white blood cells, infection-fighting cells, platelets, haemoglobin, kidney function, and liver markers
- People who are willing to take part and have signed a consent form
Who may not be able to join:
- People in whom, during surgery, the targeted part of the liver does not show a clear boundary after blood supply is blocked, or whose liver already glows too brightly before a special dye (ICG) is injected during the procedure
- People whose liver has poor reserve capacity, measured by a specific liver function test (ICG R15 of 20% or more)
- People with serious heart or lung conditions that mean they cannot safely have a general anaesthetic or surgery
- People with a moderate or large amount of fluid build-up in the abdomen or around the lungs that is causing symptoms
- People who have active bleeding or problems with blood clotting
- People who have a condition where the liver is not filtering toxins properly, affecting brain function (hepatic encephalopathy)
- People who are allergic to the dye ICG
- People who have had bleeding in the stomach or digestive tract in the past 6 months, or who have a clear risk of this happening
- People with severely enlarged veins in the oesophagus or stomach that need medical treatment
- People with clear evidence of severely reduced lung function, such as pulmonary fibrosis
- People with any significant health or test result abnormalities that the trial doctors believe could affect the safety of the study
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: Hong Wu, Professor, West China Hospital
Phone: 18980601958
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
Fluorescence imaging effect of the live
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.