Manchester Royal Infirmiary
Manchester, M13 9WL, United Kingdom
NCT Number: NCT07192731
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
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Manchester, M13 9WL, United Kingdom
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
General:
Cardiovascular fitness related exclusions:
Tumour-related exclusions:
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
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.
Time frame: 30 days
Episode-related complications of IRE using the Clavien-Dindo system and the comprehensive complication index (CCI)
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.
Time frame: 6 months
Re-ablation and modality.
Time frame: 12 months
Appearance of new lesions in liver, lungs, peritoneum or elsewhere (other) on follow-up.
Time frame: 12 months
Any further liver-directed, anti-cancer intervention including TACE and SIRT
Time frame: 12 months
Progression-free and overall survival at 12 months from time of IRE.
Time frame: 12 months
Local progression at site of IRE-treated lesion.
Time frame: 6 months
Any use of chemotherapy after IRE.
Time frame: within 7 days prior to procedure
Effect of intervention on quality of life as assessed by EQ-5D-5
Time frame: 7 days
Effect of intervention on quality of life as assessed by EQ-5D-5
Time frame: 6 months
Effect of intervention on quality of life as assessed by EQ-5D-5
Contact information is provided by the study sponsor or research team.
Angiodynamics, Inc.
Industry
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
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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