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Low dose long course peg IFN- alpha- 2b(45 uG) prospective, randomized, controlled, and open trial in the treatment of HBV related hepatocellular carcinoma

Low dose long course peg IFN- alpha- 2b(45 uG) prospective, randomized, controlled, and open trial in the treatment of HBV related hepatocellular carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047874
Enrollment
Unknown
Registered
2021-06-27
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-03-07

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

Conditions

Hepatitis B related hepatocellular carcinoma

Interventions

Group one:PD1 + targeted drug + PEG-IFN- a- 2b(45 µ g) + nucleoside analogues
Group two:Targeted drug + PEG-IFN- a- 2b(45 µ g) + nucleoside analogues
Group three:PD1 + targeted drugs + nucleoside analogues
Group four:PD1+PEG-IFN-a-2b+Nas
Group five:Nucleoside analogues
Group six:Useless medicine

Sponsors

The First Affiliated Hospital of Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient must sign the informed consent and voluntarily accept the follow-up for at least 48 weeks; 2. Aged 18 to 75 years, gender is not limited; 3. Patients diagnosed with stage IV in accordance with the "Guidelines for the Diagnosis and Treatment of Primary Liver Cancer (2020 Edition)" of the Chinese Society of Clinical Oncology; 4. HBsAg positive.

Exclusion criteria

Exclusion criteria: 1. Child-Pugh rating C; 2. Neutrophil count <0.5x10^9/L, or platelets <25x10^9/L; 3. A clear diagnosis of patients with anxiety or depression; 4. Pregnant women and lactating women; 5. Diabetic patients with poor blood sugar control; 6. Patients with poorly controlled hypertension and blood pressure; 7. The investigator believes that there are any other factors that are not suitable for inclusion or that affect subjects participating in or completing the trial.

Design outcomes

Primary

MeasureTime frame
Imaging examination of liver;

Secondary

MeasureTime frame
routine blood test;liver function;Hepatitis B DNA;hepatitis B surface antigen quantification;alpha-fetoprotein;

Countries

China

Contacts

Public ContactLu Xiaobo

The First Affiliated Hospital of Xinjiang Medical University

Xjykdluxiaobo@126.com+86 15999176213

Outcome results

None listed

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