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:
- Adults aged 18 or older who are expected to live for at least one year
- People who have been diagnosed with liver cancer (hepatocellular carcinoma), confirmed through specific imaging results, a tissue biopsy, or through a combination of liver scarring (cirrhosis) and a raised level of a liver cancer marker in the blood (AFP above 400)
- People whose cancer has not spread into major blood vessels or to other parts of the body, and who have up to 5 liver tumours, where at least one tumour is between 2 and 5 cm in size and none are larger than 5 cm
- People whose tumour location is considered safe and technically suitable for a needle-based heat treatment (percutaneous thermal ablation), as assessed by a specialist doctor
- People who are generally well enough to carry out most daily activities, with a physical ability rating of 0–2 on a standard medical scale (ECOG 0–2) (confirm with trial site)
- People whose blood clotting levels meet specific thresholds: platelets at or above 50,000/μL and a clotting measure (INR) at or below 1.8, or correctable to that level
- People who are able to have a contrast-enhanced CT or MRI scan
- People who are willing and able to give informed consent to take part
Who may not be able to join:
- People who have already had a previous treatment (such as ablation, chemoembolisation, radiation, or surgery) to the target tumour or to a tumour within 1 cm of it
- People who have more than 5 liver tumours, or where any tumour cannot be fully treated with ablation
- People with uncontrolled liver failure, including ongoing confusion caused by liver disease (hepatic encephalopathy)
- People with blood clotting problems that cannot be corrected, or other reasons why a needle-based liver procedure would not be safe
- People who cannot safely have contrast-enhanced imaging — for example, due to severe kidney disease without dialysis, or a contrast dye allergy that cannot be managed with pre-treatment medication
- People with an active infection anywhere in the body
- People who are pregnant
- People who would not be able to attend the required follow-up scans after treatment
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: Andrea Borsic, PHD, NE Scientific INC
Phone: 1 603 667 0283
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 Tumor Progression; Technical Effectiveness
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.