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Clinical Trials/JPRN-UMIN000005229
JPRN-UMIN000005229
Completed
Phase 2

PhaseII study of trancatheter arterial chemoembolizaion with miriplatin for hepatocellular carcinoma -Compared with retrospective historical cohort study with epirubicin hydrochloride- - PhaseII study of TACE with miriplatin for HCC

ara Medical University, Department of Radiology0 sites33 target enrollmentMarch 11, 2011

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
ara Medical University, Department of Radiology
Enrollment
33
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 11, 2011
End Date
March 1, 2014
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
ara Medical University, Department of Radiology

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Patients who have medical history of hypersensitivity of platinum\-containing drug. 2\) Patients who have medical history of hypersensitivity of iodine containing agent and/or contrast material. 3\) Extrahepatic metastasis. 4\) Bile duct invasion or vascular invasion. 5\) Patients after HCC is ruptured. 6\) Patients who have medical history of surgical reconstruction of the biliary tract or endoscopic biliary treatment. 7\) Patients who have moderate or severe pleural effusion or ascites to be unresponsive to therapy. 8\) Severe arterioportal shunt or arteriovenous shunt in the liver. 9\) Patients with following severe complicating disease. \- Patients who are difficult to control heart failure, angina or arrhythmia despite treatment \- Cardiac infarction within 6 months of onset \- Renal failure \- Active infections(except viral hepatitis) \- Active gastrointestinal bleeding \- Active duplicative cancer \- Hepatic encephalopathy or severe mental illness 10\) Patients who are pregnant, lactating or are suspected to be pregnant. 11\) Patients who are concluded to be inappropriate to participate in this study safety by their physicians.

Outcomes

Primary Outcomes

Not specified

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