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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01447667
Other study ID # MRE
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2011
Est. completion date December 2022

Study information

Verified date November 2023
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine: - The efficacy of MRE score as a predictor of HCC recurrence within 2 years after RFA treatment - The efficacy of each indicator (MRE score, non-invasive serum markers) compared to the gold-standard histology score predicting hepatic fibrosis


Description:

To evaluate whether MRE score reflecting hepatic fibrosis can predict the recurrence of HCC within 2 years after RFA treatment - Local recurrence/intrahepatic distant recurrence - Multivariable analysis including several related factors to find whether MRE score is an independent predictor of HCC recurrence even after adjusting other factors (etiology of liver disease, size of HCC, vessel invasion, HBsAg titer, etc.) To find the efficacy of each indicator (MRE score, non-invasive serum markers) compared to the gold-standard histology score predicting hepatic fibrosis.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Diagnosed as single hypervascular hepatocellular carcinoma initially - AJCC stage I HCC - Child-Pugh class A - Planning radiofrequency ablation for HCC - Voluntary agreement for this study Exclusion Criteria: - Decreased kidney function (GFR < 70 mL/min/kg) - Contraindication to MRI (pacemaker, defibrillator) - Contrast media hypersensitivity - Other primary malignancy - Acute viral hepatitis - Prior history of liver transplantation - Thrombosis in splenic vein or portal vein - Patients who were enrolled to other clinical trials within 4 weeks - Other severe chronic disease or psychiatric disease - Pregnant or milk-feeding women - Patients with coagulopathy, high risk of bleeding for the liver biopsy - Patients who disagree to participate in this study

Study Design


Intervention

Procedure:
Magnetic resonance elastography
Magnetic resonance elastography before RFA and Liver biopsy of 2 HCC tissue and 2 non tumor liver parenchyma tissue

Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients who experienced HCC recurrence after RFA To see whether MRE score reflecting hepatic fibrosis predicts the recurrence of HCC within 2 years after RFA treatment within 2 years after RFA procedure
Secondary Sensitivity and specificity of each indicator of hepatic fibrosis compared to the gold-standard histology score To find efficacy of each indicator (MRE, noninvasive serum markers such as APRI, P2/MS) compared to the gold-standard histology score in predicting hepatic fibrosis 2 years after RFA
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