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Randomized contorol trial of transarterial chemoinfusion with cisplatin-lipiodol susupension or miriplatin-lipiodol suspension for advanced HCC

Randomized contorol trial of transarterial chemoinfusion with cisplatin-lipiodol susupension or miriplatin-lipiodol suspension for advanced HCC - Randomized contorol trial of transarterial chemoinfusion for advanced HCC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003452
Enrollment
100
Registered
2010-05-01
Start date
2010-05-01
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

Hepatocellular carcinoma

Interventions

Miriplatin-lipiodol suspension group:Powdered miriplatin(70mg) suspended in lipiodol(6ml) is injected through the catheter selectively introduced into the hepatic artery,The doses of suspension are de

Sponsors

First Department of Internal Medicine,Gifu University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Histologically or clinically comfirmed Hepatocellular carcinoma 2)Patients diagnosed as stage2-3 3)Interval of 4 weeks or over between last treatment and present therapy 4)Child-pugh is A or B 5)No indication for surgical resection or local ablation 6)PS is 0,1 or 2 7)Sufficient functions of main organ(bone marrow,kidney,heart)and conditions filled a following criteria 1 WBC>=2,000 /mm3,<=10,000 /mm3 2 Plt>=50,000 /mm3 3 Hb>=8.0 g/dL 4 T-Bil<=3.0 mg/dL 5 PT>=50% 6 Creatinine<=1.5 mg/dL 7 BUN<=35 mg/dL 8)Age is more than 20 years old and below 80 years old 9)Patients obtained written infoemed consent

Exclusion criteria

Exclusion criteria: 1)Patienta with sever co-morbidity such as cardiac failure or renal failure 2)Patienta with a medical history of severe hypersensitivity 3)Patients who are pregnant,lactating or are suspected to be a pregnant 4)Patients who are concluded to be inappropriate to participate in this study by their physitians

Design outcomes

Primary

MeasureTime frame
Response rate

Secondary

MeasureTime frame
Overall survival Safety

Countries

Japan

Contacts

Public ContactKoji Takai

Gifu University Hospital First Department of Internal Medicine

koz@gifu-u.ac.jp058-230-6000

Outcome results

None listed

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