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Prospective randomized study of Microwave Ablation combined with Transcatheter Arterial Chemoembolization in Treatment of Large Hepatocellular Carcinoma with liver cirrhosis

Prospective randomized study of Microwave Ablation combined with Transcatheter Arterial Chemoembolization in Treatment of Large Hepatocellular Carcinoma with liver cirrhosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015590
Enrollment
Unknown
Registered
2018-04-10
Start date
2018-04-16
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Hepatocellular Carcinoma

Interventions

Intervention Group:MWA followed by TACE
Control Group:MWA alone

Sponsors

Department of Interventional Oncology,Renji hospital, School of Medicine,Shanghai JiaoTong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Patients with primary liver cancer aged 18 to 75 years, the expected survival of at least 3 months; (2) Large hepatocellular carcinoma with no more than 3 tumors and a maximum diameter of more than 5 cm and less than 10 cm, pathologically characterized by primary hepatocellular carcinoma (HCC); (3) No portal vein tumor thrombus; (4) Child-Pugh liver function classification A or B; ECOG physical status score of 2; (5) Patients with cirrhosis who show one of the following, such as mild ascites, endoscopic esophageal varices, MELD score of not less than 12; (6) Hematological examination (platelet count> 40×10^9/L, INR <2.0); (7) Renal function (creatinine <2.0 mg/dL); (8) White blood cell count=3.0×10^9/L; (9) Hemoglobin = 8.5g/dl.

Exclusion criteria

Exclusion criteria: (1) Diffuse liver cancer; (2) Cholangiocarcinoma; (3) With portal vein tumor thrombus; (4) Hepatic vein tumor thrombus; (5) lymph node metastasis and extrahepatic metastasis; (6) With clinical hepatic encephalopathy, refractory ascites or uncorrectable coagulation disorders (7) Women in pregancy or lactation; (8) Previously allergic to iodized oil and chemotherapy drugs.

Design outcomes

Primary

MeasureTime frame
Overall Survival(OS);

Secondary

MeasureTime frame
Time of Tumor Disease Progression (TTDP);Feasibility of procedure;Feasibility of safety;Local Tumor Progression;Intrahepatic Distant Recurrence;Extrahepatic Metastases;

Countries

China

Contacts

Public ContactZhai B

Department of Interventional Oncology, Renji hospital, School of Medicine,Shanghai JiaoTong University

zhaiboshi@sina.com+86 13918056019

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026