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Transarterial Chemoembolization (TACE) with or without Sequential Cryoablation in Hepatocellular Carcinoma of BCLC B:a Multicentral Randomized Controlled Trial

Transarterial Chemoembolization (TACE) with or without Sequential Cryoablation in Hepatocellular Carcinoma of BCLC B:a Multicentral Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16007915
Enrollment
Unknown
Registered
2016-02-13
Start date
2016-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

hepatocellular carcinoma

Interventions

A:transarterial chemoembolization
B:Transarterial Chemoembolization (TACE) with Sequential Cryoablation

Sponsors

The First Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. CT, MRI and AFP combined with clinical or pathological diagnosis of hepatocellular carcinoma; 2. Prior informed consent; Be able to follow the visit/treatment rules according to the research programs; 3. Generally in good condition, adequate bone marrow, liver and renal function; 4. ECOG Performance Status of 0-2; 5. Advanced stage HCC/ BCLC B stage; 6. Hepatitis B history or HBsAg positive; 7. Patients without previously surgery, local-regional therapies (radiofrequency ablation, et al), or liver transplantation; 8. Aged 18 to 65 years; 9. Child Pugh class A/B (== 100*10^9/L; ALT and AST =30g/L; Total bilirubin =<34 mmol/L.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Extrahepatic metastasis, or tumor thrombosis invasive venous system; 3. Any contraindications for hepatic embolization procedures(known renal failure/insufficiency requiring hemo-or peritoneal dialysis); 4. Patients with prior malignancy were ineligible for the study, with the exception of those who had been disease free for longer than 5 years; 5. Patients with liver transplantation.

Design outcomes

Primary

MeasureTime frame
3year overall survival rate;

Secondary

MeasureTime frame
Time to progression;distant metastasis rate;

Countries

China

Contacts

Public ContactJia-ping Li
jpli3s@126.com+86 13352890908

Outcome results

None listed

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