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Efficacy and significance of antiviral therapy for unresectable Hepatitis B Virus-related hepatocellular carcinoma

A randomized, controlled study to evaluate the efficacy and significant of the anti-virus therapy in the unresectable Hepatitis B Virus-related hepatocellular carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-08000292
Enrollment
Unknown
Registered
2008-11-18
Start date
2008-11-01
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

unresectable HBV-related HCC

Interventions

Group B:without any anti-virus therapy
Group A:Anti-HBV-virus therapy

Sponsors

Shanghai Eastern Hepatobiliary Surgery Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Identify patients with HCC in accordance with the clinical diagnostic criteria of HCC passed at the Chinese Eighth National Live Cancer Academic Conference. Patients with HCC shall be diagnosed with or without pathology. It is not appropriate to perform liver resection operation; 2. serum positive HBsAg >=6 months; 3. Criteria of liver function: Child A or B level, serum total bilirubin =8.5g/dl, PT-INR6 seconds of normal value; 5. No dysfunction in major organs; Blood routine, kidney function, cardiac function and lung function are basically normal; 6. Patients who can understand this trial, male or female, aged 18-70 voluntarily participate in clinical trials and have signed information consent.

Exclusion criteria

Exclusion criteria: 1. Patients with apparent cardiac, pulmonary, cerebric and renal dysfunction, which may affect the treatment of liver cancer. 2. Patients with other diseases which may affect the treatment mentioned here. 3. Patients with medical history of other malignant tumours. 4. Subjects participating in other clinical trials. 5. Women in pregnancy and breast-feeding.

Design outcomes

Primary

MeasureTime frame
clinical symptom, laboratory examination (HBV-M, HBV-DNA, AFP, liver function), quality of life;

Secondary

MeasureTime frame
time of tumor progress(TTP), overall survival rate(OS);

Countries

China

Contacts

Public ContactHu Heping
hp-hu@medmail.com.cn+86 021 25070868

Outcome results

None listed

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