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Comparison of Sorafenib and DEB-TACE in patients wth hepatocellular carcinoma refractory to conventional TACE.

Not Applicable
Conditions
hepatocellular carcinoma
Registration Number
JPRN-UMIN000014999
Lead Sponsor
Musashino Red Cross Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

1)Patiets that written agreement of participation for this study was not obtained. 2)Patients whose HCC with invasion of stem of portal vein. 3)Patients with uncontrollable ascites. 4)Patients whose TMN stage of HCC is IVb. 5)Patients whose Child-Pugh is B or C. 6)Pregnant patiients. 7)Patients with iodine hypersensitivity. 8)Patients who were estimated that study entry is inappropriate by the responsible physician.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
overall survival rate
Secondary Outcome Measures
NameTimeMethod
progression-free survival response rate
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