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Effect of pegylated interferon alpha-2b plus ribavirin therapy on cirrhotic patients with chronic hepatitis C virus infection

Effect of pegylated interferon alpha-2b plus ribavirin therapy on cirrhotic patients with chronic hepatitis C virus infection

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-14005561
Enrollment
Unknown
Registered
2014-11-29
Start date
2013-11-01
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

Hepatitis C cirrhosis

Interventions

1:pegylated interferon alpha-2b plus ribavirin
1:symptomatic treatment
2:symptomatic treatment

Sponsors

302 Military Hospital of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Cirrhotic patients with chronic HCV infection based on diagnostic criteria of 2004 China clinical practice guidelines of chronic hepatitis C; 2. Males or females with age from 18 to 60 years old, capable of signing the informed consent; 3. Patients with HCV RNA more than 10^3 IU/ml; WBC more than 2.0*10^9/L; NE more than at least 1.0*10^9/L; PLT more than 60*10^9/L; HGB more than 100 g/L; 4. Patients with Child-Pugh A or B; BIL less than 2*ULN;BMI less than 28 kg/m^2.

Exclusion criteria

Exclusion criteria: a.Patients combined with other virus infection, liver failure, Child-Pugh C class, liver tumor, cardio-cerebrovascular disease, The blood system disease, or psychiatric disorders; b.Patients enrolled in other clinical trials; c.Patients with poor compliance or other factors which may lead to mistakes in determine of effect or safety; d.Allergy, pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
HCV RNA undetectable rate;histological improvment rate;

Secondary

MeasureTime frame
safety evaluation;HCC rate;liver function decompensated rate;

Countries

China

Contacts

Public ContactChen Guofeng
guofengchen302@163.com+86 10 66933427

Outcome results

None listed

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