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Polymorphisms of Fibrosis-Relating Genes on Outcome of HCV-Related Chronic Liver Disease

K

Kaohsiung Medical University

Status

Completed

Conditions

Chronic Liver Disease
Fibrosis

Treatments

Genetic: cytokine polymorphism
Genetic: cytokine
Genetic: cytokine polymorphisms

Study type

Interventional

Funder types

Other

Identifiers

NCT00629603
KMUH-IRB-950347

Details and patient eligibility

About

Hepatitis C virus (HCV) infection causes different disease spectrum ranging from minimal progressive liver disease to cirrhosis or hepatocellular carcinoma. Evidence indicates that host genetic factor may play a role in determining disease progression. It is known that many cytokine polymorphisms affect disease progressin via increasing hepatic fibrosis that are key factors in progressing liver injury. By combinations of fibrosis-relating gene polymorphisms, this study aims to identify patients with high risk for progressive liver disease. These patients need intensive therapy to decrease morbidity and mortality of chronic HCV-related liver disease.

Full description

Determination of the following fibrosis-relating gene polymorphisms in HCV-related chronic liver disease and HCC will be performed: TNF-α , TNF-β, Factor V Leiden, TGF-β1, PDGF-B gene, Angiotensinogen (AT),Angiotensin converting enzyme (ACE), microsomal epoxide hydrolase (mEH) and glutathione-S-transferase (GST).

Enrollment

600 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with anti-HCV positive

Exclusion criteria

  • Anti-HCV-negative patients

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

600 participants in 1 patient group

cytokine polymorphisms, HCV infection
Experimental group
Description:
Relate the fibrosis cytokine gene polymorphisms with disease severity of HCV-related chronic liver disease
Treatment:
Genetic: cytokine polymorphisms
Genetic: cytokine
Genetic: cytokine polymorphism

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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