Liver Cancer Trial, Recruiting NCT06909708 Sponsor: Zhongda Hospital Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT06909708
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 7 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Zhongda Hospital
Registry
ClinicalTrials.gov
Start date
3 April 2025
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Time to progression (TTP)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov