A Study to Evaluate Efficacy and Safety of TheraSphere and Resection Combination Therapy in Patients With Single Large ((> 5cm, Long Diameter ) Hepatocellular Carcinoma : Exploratory Trial

NACompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

January 30, 2018

Primary Completion Date

June 2, 2021

Study Completion Date

June 2, 2021

Conditions
Carcinoma, Hepatocellular
Interventions
DEVICE

Theraspere

Prior to the administration of TheraSphere, the patient should undergo hepatic arterial catheterization using balloon catheterization or other appropriate angiographic techniques to prevent extrahepatic shunting. Following the placement of the hepatic catheter, 75 MBq to 150 MBq (2 mCi to 4 mCi) of Tc-99m MAA is administered into the hepatic artery to determine the extent of A-V shunting to the lungs and to confirm the absence of gastric and duodenal flow. When the possibility of extrahepatic shunting has been evaluated and the patient deemed acceptable for treatment, TheraSphere may be administered.

Trial Locations (1)

Unknown

Seoul National University Hospital, Seoul

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

BTG International Inc.

OTHER

collaborator

Seoul National University Hospital

OTHER

lead

MedicalExcellence

OTHER