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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05449873
Other study ID # 2107-087-1235
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 18, 2021
Est. completion date July 30, 2023

Study information

Verified date October 2022
Source Seoul National University Hospital
Contact Hyun Hee Lee
Phone 82-2-2072-4177
Email redlion55@naver.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate local tumor progression rate at 12 months after no-touch percutaneous radiofrequency ablation using combined energy delivery mode and triple cooled electrodes


Recruitment information / eligibility

Status Recruiting
Enrollment 73
Est. completion date July 30, 2023
Est. primary completion date July 30, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years to 85 Years
Eligibility Inclusion Criteria: - Child-Pugh Class A or B - chronic hepatitis B or chronic hepatitis C or liver cirrhosis - presence of recurrent hepatocellular carcinoma (HCC) after locoregional treatment confirmed by pathology or imaging studies including contrast enhanced computed tomography (CT) or magnetic resonance imaging (MRI) according to Liver Imaging Reporting and Data System (LI-RADS) v2018 - single lesion less than or equal to 5 cm, or up to 3 lesions, each greater than less than or equal to 3 cm at the time of locoregional treatment Exclusion Criteria: - number of recurrent HCCs, equal or more than 3 - largest recurrent HCC size over 3 cm - presence of vascular invasion by HCC - platelet count less than 40,000 per mm3 or International Normalized Ratio (INR) prolongation over 50% - presence of extrahepatic metastasis

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Radiofrequency ablation using combined bipolar and monopolar energy deliver with Triple Cooled-Wet electrodes
Radiofrequency ablation will be performed by using triple cooled-wet electrodes. Two or three electrodes will be places around the tumor under ultrasonography (US)-computed tomography (CT)/magnetic resonance (MR) fusion tool guidance. The electrodes will be cooled with saline, and radiofrequency (RF, bipolar mode and switching monopolar mode) will be applied to two of three electrodes at the same time for about 6 to 30 minutes depending on the tumor size. The temperature will be maintained at 90-100 °C.

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (2)

Lead Sponsor Collaborator
Seoul National University Hospital RF medical

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Local tumor progression rate Evaluate local tumor progression by follow-up computed tomography (CT) or magnetic resonance imaging (MRI) with alpha-fetoprotein (AFP) level 12 months after radiofrequency ablation
Secondary Disease-free survival Evaluate disease-free survival by available clinical information and follow-up computed tomography or magnetic resonance imaging with alpha-fetoprotein level 12 moths after radiofrequency ablation
Secondary Technical success rate Evaluate technical success defined as complete ablation of the index tumor with safety margin, equal or larger than 3 mm on 1 month follow-up CT. 1 month after radiofrequency ablation
Secondary Overall survival Evaluate overall survival by available clinical information and follow-up 12 moths after radiofrequency ablation
Secondary Complication rate Evaluate the presence of major or minor radiofrequency ablation related complications on follow-up computed tomography or magnetic resonance imaging. 1, 3, 6, 9, 12 months after radiofrequency ablation.
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