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NCT Number: NCT07192731

International Study on Treatment of Liver (HCC) Patients With IRE

Procedural data will be recorded from patients with liver lesions from hepatocellular cancer who have been assessed by an appropriately constituted MDT (or equivalent) as appropriate to receive irreversible electroporation

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Manchester Royal Infirmiary

Manchester, M13 9WL, United Kingdom

Location contact

Ajith Siriwardena, MD FRCS

CONTACT

[email protected]

+44

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 18 years and over, able to provide informed consent and with clinical diagnosis of an HCC. Tissue confirmation of HCC prior to treatment is not standard of care and is therefore not required for this study.
  • Child-Pugh A up to A6.
  • Eastern Co-operative Oncology Group (ECOG) Score ≤ 2.
  • Rockwood Frailty Score ≤ 3.
  • Serum bilirubin < 30 µmol/L.
  • Serum creatinine < 150 µmol/L.
  • No extrahepatic metastases
  • IRE can be used for up to 3 tumours < 3cm in size. Other forms of ablation can be combined with IRE in the same sitting but not for the same lesion. IRE can also be combined with surgical resection.

Exclusion criteria

General:

  • Patients involved in other research studies.
  • Patients under the age of 18 years.
  • Inability to give informed consent.
  • Patients who are pregnant.
  • Child-Pugh B or C.
  • Patients with an ECOG status of > 2 at time of recruitment.
  • Rockwood Frailty Score > 3
  • Impaired renal function (serum creatinine > 150 µmol/L)
  • Accepted exclusions to IRE from consensus criteria including:
  • Platelet count < 50x109 U/L.
  • International normalised ratio (INR) for blood clotting > 1.7.
  • Prior hepatic tumour ablation.

Cardiovascular fitness related exclusions:

  • History of ventricular arrhythmia.
  • Implanted pacemaker or defibrillator.
  • Congestive cardiac failure NYHA Class ≥ 3.

Tumour-related exclusions:

  • Tumour ≥ 3 cm in size.
  • Extrahepatic metastatic disease.
  • Jaundice (serum bilirubin > 30 µmol/L).
  • MDT recommends use of thermal ablation for any given lesion.

Treatment and study plan

Irreversible Electroporation

Device

Irreversible electroporation (IRE) is a procedure which involves the passage of short intense electrical pulses between probes to destabilize cell membranes by creating "nanopores" which leads to cell destabilisation and cell death.

IRE can be used to selectively damage cancerous cells whilst sparing adjacent supporting connective tissue in vessels and bile ducts allowing a more targeted treatment compared to other types of ablation. IRE also avoids the heat-sink phenomenon which compromises the effectiveness of thermal ablation and possibly reduces the risks of biliary injury.

Other names: nanoknife

Primary outcomes

  1. Target Tumour Eradication

    Time frame: 6 months

    The percentage of target tumours successfully eradicated 6 months after the initial IRE procedure, according to RECIST and PERCIST criteria. This is based on a per-lesion analysis.

Secondary outcomes

  1. Complications of IRE: Episode-related complications:

    Time frame: 30 days

    Episode-related complications of IRE using the Clavien-Dindo system and the comprehensive complication index (CCI)

  2. Complications of IRE: Intervention for local liver-related complications of IRE

    Time frame: 12 months

    Any intervention for local liver-related complications of IRE within 12 months of procedure. Interventions will be categorised as radiological, surgical or medical.

  3. Oncological outcomes: Incomplete ablation requiring further intervention

    Time frame: 6 months

    Re-ablation and modality.

  4. Oncological Outcome: Progression at site of ablation

    Time frame: 12 months

    Appearance of new lesions in liver, lungs, peritoneum or elsewhere (other) on follow-up.

  5. Oncological outcome: Further anti-cancer intervention

    Time frame: 12 months

    Any further liver-directed, anti-cancer intervention including TACE and SIRT

  6. Oncological Outcome: Survival (Progression-free & overall)

    Time frame: 12 months

    Progression-free and overall survival at 12 months from time of IRE.

  7. Oncologic Outcomes: local progression

    Time frame: 12 months

    Local progression at site of IRE-treated lesion.

  8. Oncologic Outcomes: Chemotherapy post-IRE

    Time frame: 6 months

    Any use of chemotherapy after IRE.

  9. Quality of life: EQ-5D-5 pre-procedure

    Time frame: within 7 days prior to procedure

    Effect of intervention on quality of life as assessed by EQ-5D-5

  10. Quality of life: EQ-5D-5 post-procedure 7 days

    Time frame: 7 days

    Effect of intervention on quality of life as assessed by EQ-5D-5

  11. Quality of life: EQ-5D-5 - 6 months

    Time frame: 6 months

    Effect of intervention on quality of life as assessed by EQ-5D-5

Study contacts

Contact information is provided by the study sponsor or research team.

Mitchell Vanderpoll

CONTACT

[email protected]

+44 7790921819

Sponsors and collaborators

Lead sponsor

Angiodynamics, Inc.

Industry

Registry information

Official study title

Treatment of LIVER-limited HepatoCellular Carcinoma (HCC) in Patients With Preserved Liver Function by IRreversible Electroporation: A Prospective, International, Multi-centre Cohort Study

Acronym: LIVERHCC-IRE

Important dates

Study start
2026
Primary completion
2028
Study completion
2029
First posted
Sep 25, 2025
Registry last updated
Oct 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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