Hepatocellular Carcinoma Clinical Trial
Official title:
Radiofrequency Ablation Using Internally Cooled Wet Electrodes in Bipolar Mode for the Treatment of Recurrent Hepatocellular Carcinoma After Locoregional Treatment: A Randomized Prospective Comparative Study
| Verified date | April 2020 |
| Source | Seoul National University Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This study was conducted to provide preliminary data for the main trial to compare efficacy between bipolar radiofrequency ablation (RFA) using twin internally cooled-wet electrodes and switching monopolar RFA using separable clustered electrodes in the treatment of recurrent hepatocellular carcinoma (HCC) after locoregional treatment.
| Status | Completed |
| Enrollment | 77 |
| Est. completion date | February 12, 2019 |
| Est. primary completion date | May 16, 2018 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 20 Years to 80 Years |
| Eligibility |
Inclusion Criteria: - radiologic or pathologic diagnosis of HCC recurrence after locoregional treatment - HCC nodules measuring 1 cm or larger and smaller than 5 cm Exclusion Criteria: - more than three HCC nodules - tumors with major vascular invasion or abutment to the central portal or hepatic vein with a diameter > 5mm - extrahepatic metastasis - Child-Pugh class C - severe coagulopathy (platelet cell count of less than 50,000 cells/mm3 or prothrombin time international normalized ratio (PT-INR) prolongation of more than 50 %) |
| Country | Name | City | State |
|---|---|---|---|
| Korea, Republic of | Seoul National University Hospital | Seoul |
| Lead Sponsor | Collaborator |
|---|---|
| Seoul National University Hospital |
Korea, Republic of,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Complication | Description and comparison of the type and incidence of major complication after RFA are assessed according to Society of Interventional Radiology (SIR) grading system in two groups. | 1 month after RFA | |
| Other | Volume of ablative zone | Volume of ablative zone on post-RFA CT or MRI in a mm3 | 3 days after RFA | |
| Other | Ablation time | RFA procedure time in each patient. | 1 day | |
| Primary | Minimum diameter of ablation zone per unit time | Minimum diameter of ablative zone per unit time on post-RFA CT or MRI in a mm. | 3 days after RFA | |
| Secondary | Technique efficacy | Technical success on 1 month follow-up imaging after RFA (no residual/progressed tumor) | 1 month after RFA | |
| Secondary | IDR rate | Cumulative intrahepatic distant recurrence (IDR) rate over 2 years after RFA | 12 months, 24 months after RFA | |
| Secondary | EM rate | Cumulative extrahepatic metastasis (EM) rate over 2 years after RFA | 12 months, 24 months after RFA | |
| Secondary | Local tumor progression (LTP) | Cumulative LTP rates in two groups in 2 years after RFA | 12 months, 24 months after RFA |
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