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Radiofrequency Ablation Using Octopus Electrodes for Treatment of Focal Liver Malignancies

Radiofrequency Ablation Using Octopus Electrodes for Treatment of Focal Liver Malignancies

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02683538
Enrollment
196
Registered
2016-02-17
Start date
2011-11-30
Completion date
2014-07-31
Last updated
2016-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cholangiocarcinoma, Hepatocellular Carcinoma, Metastasis

Keywords

RFA

Brief summary

The purpose of this study is to evaluate the clinical feasibility and short-term outcome of switching monopolar RFA using a separable cluster electrode in patients with primary and secondary liver malignancies.

Detailed description

Radiofrequency ablation (RFA) is one of minimal invasive treatment methods and it has been showing comparable overall survival with surgery in early or small hepatocellular carcinomas (HCCs) and better cost-effectiveness. However, it is suffering from high local tumor progression (LTP) rate. To reduce LTP rate, creation of large ablative zone has been attempted in various strategies. A separable cluster electrode is a new type of RFA electrode. It consists of three individual applicators and the applicators can be incorporated as a single handle such as a cluster electrode, and can be separated as three electrodes, depending on operators' needs. It allows high flexibility to operators and the preclinical results were promising. Herein, we want to evaluate the clinical feasibility of the electrodes by observing major complication rates, technical success rate and 12-months LTP rate.

Interventions

DEVICESeparable cluster electrode (Octopus®)

Patients undergo RFA under ultrasound guidance, and separable cluster electrodes are used for RFA in monopolar switching mode, using multiple overlapping technique to create larger ablative zones.

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hepatic malignancies diagnosed on biopsy OR * Typical imaging features of hepatocellular carcinoma (HCC) on computed tomography (CT) or magnetic resonance imaging (MRI) according to AASLD guideline * Typical imaging feature of metastasis on CT or MRI AND * 1\ 5 tumors equal to or smaller than 5cm in the liver * no direct contact with or invasion into the hepatic hilar structures or inferior vena cava (IVC) * Eastern Cooperative Oncology Group performance status of 0 * Patients who signed informed consent

Exclusion criteria

Patients with any of followings are excluded. * Patients with uncontrolled coagulopathy * Patients with Child-Pugh classification C * Patients with tumor invasion in major portal vein or hepatic vein branch * Extrahepatic metastasis

Design outcomes

Primary

MeasureTime frameDescription
Major complication rate after Radiofrequency ablation (RFA)30 days after RFARates of major complication according to Society of Interventional Radiology (SIR) grading system, which refers to an event that leads to substantial morbidity and disability (SIR classification C-E).

Secondary

MeasureTime frameDescription
Technical success1 day after RFATechnical success addresses that the tumor was treated according to protocol and completely covered by ablative zone on pre-RFA image and post-RFA image side-by-side comparison.
Local control rate12 months after RFARate of local tumor progression after RFA

Other

MeasureTime frameDescription
total procedure time1 day after RFAtotal procedure time per patients was recorded.
Ablative zone volume1 day after RFAablative zone volume measurement for each tumor on post-RFA cross sectional imaging

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026