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Combination Therapy of RFA and Miriplatine Versus RFA for HCC larger than 3cm

Combination Therapy of RFA and Miriplatine Versus RFA for HCC larger than 3cm - Combination Therapy of RFA and Miriplatine Versus RFA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004523
Enrollment
50
Registered
2010-11-09
Start date
2010-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HCC larger than 3cm

Interventions

Combination therapy of RFA with hepatic arterial infusion group RFA-alone group

Sponsors

Osaka city University Graduate School of Medicine Department of Hepatotlogy
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: I.Patients with primary hepatocellular carcinoma diagnosed by clinical or histological(angiography, CT, etc.) study II.Hepatocellular carcinoma larger than 3cm, technically possible for radiofrequency ablation (except cases of liver resection), aim to complete cure or mass reduction III.Organ function is maintained. The following clinical and laboratory criteria must be satisfied. - Child-Pugh classification A or B patients - Degree of liver failure (Liver damage) A or B patients - Platelet count: more than 30,000 / mm3 IV.Patients are expected to survive more than three months from start of treatment at least V.General conditions ECOG (Japan Clinical Oncology Group) Performance Status 0,1, or 2 VI.Patients obtained writtten informed consent

Exclusion criteria

Exclusion criteria: I.Patients who are considered not to participate in the study by physicians II.Patients with moderate or severe infections III.Patients with uncontrolled diabetes or obstruction IV.Pregnancy, nursing, or woman who may become pregnant V.Patients with a history of hypersensitivity to drugs or contrast agents containing iodine VI.Patients with a history of myocardial infarction within 3 month

Design outcomes

Primary

MeasureTime frame
Local recurrence and prognosis

Countries

Japan

Contacts

Public ContactShuji Iwai

Osaka City University Graduate School of Medicine Department of Hepatotlogy

s-iwai@med.osaka-cu.ac.jp06-6645-3811

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026