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Role and molecular mechanism of susceptibility gene and lncRNA in HCV related liver fibrosis and hepatocellular carcinoma

Role and molecular mechanism of susceptibility gene and lncRNA in HCV related liver fibrosis and hepatocellular carcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-COC-17010947
Enrollment
Unknown
Registered
2017-03-22
Start date
2015-01-01
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

chronic hepatitis C

Interventions

Control:no
HCV (F<2):no
HCV (2):no
HCV-HCC:no

Sponsors

The Third Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Baseline biopsy are consistent with the diagnosis of CHC; 2. Baseline CT/MRI are consistent with diagonosis of HCC; 3. Compensated liver diseases (Child-Pugh: A).

Exclusion criteria

Exclusion criteria: 1. History or other evidence of decompensated liver disease (Coagulopathy, hyperbilirubinemia, hepatic encephalopathy, hypo-albuminemia, ascites, and bleeding from esophageal varices are conditions consistent with decompensated liver disease; patients with cirrhosis in Child-Pugh score > 6); 2. Co-infection with active hepatitis B, hepatitis D and/or human immuno- deficiency virus (HIV); 3. Neutrophil count 100 ng/mL; 5. Pregnant or breast-feeding females (positive pregnancy test immediately prior to initiation of therapy), male partners of women who are to be pregnant; 6. Serum creatinine level > 1.5 ULN at screening; 7. History of drug allergy on IFN or any compound of IFN; 8. History of drug and alcohol abuse; 9. History of autoimmune disease; History of severe psychiatric disease, especially depression; History of thyroid disease poorly controlled on prescribed medications; History of severe retinal disease; History of malignant tumor; History of chronic pulmonary disease with insufficient function; History of severe cardiac or digestive disease; History of disease aggravating anaemia; 10. Other issues that investigators consider unsuitable for this trial.

Design outcomes

Primary

MeasureTime frame
ALT;AST;

Countries

China

Contacts

Public ContactYuemin Nan

Third Hospital of HeiBei Medical University

nanyuemin@163.com+86 18533112266

Outcome results

None listed

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