Pharmacogenomics Study on IL28B Genetic Variants in Chinese Children With Hepatitis C Virus Infection
NCT ID: NCT01607021
Last Updated: 2015-08-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
200 participants
OBSERVATIONAL
2012-04-30
2015-12-31
Brief Summary
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Detailed Description
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The use of combination treatment with interferon-alpha and ribavirin were recommended in the treatment of chronic hepatitis C in children, SVR in children with genotype 1 ranged from 44% to 59%. SVR in children with genotype 2 and 3 was more than 90%. But both interferon and ribavirin have significant side effects which affect compliance, such as: repeated flu like symptoms, leukopenia and anemia, moderate weight loss, behavioural problems, thyroid dysfunction and transient deceleration of the growth rate. In addition, approximately 50% of children infected with genotype 1 do not respond to therapy.
Recent work has highlighted that single nucleotide polymorphisms (SNPs) around the IL28B gene have been identified as strong predictors of spontaneous and treatment-induced HCV clearance in adults, especially Rs 12979860 and Rs 8099917. A recent article in Hepatology also reported that interleukin (IL)-28B C/C genotype in the child was associated with spontaneous clearance of hepatitis C virus (HCV) genotype 1 infection. All this reports show that Genetic Variation in Interleukin-28B Locus is associated with the procession of CHC.
The aim of this study was to study the association between genetic variation in IL-28B and the development of CHC in Chinese children, such as: HCV viral load, serum alanine aminotransferase, histological change and the response to the treatment with interferon-alpha and ribavirin.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Chinese children with HCV RNA positive
A sample of 200 children with a recent confirmation of anti-HCV-antibody positive and HCV RNA positive. All the children were treated with antiviral therapy, and the course of treatment depend on HCV Viral genotyping(ie, genotype 1,2,3,4 subtypes).
Primary Outcome Measures:
Virologic response \[ Time Frame: Weeks 2, 4, 6, 8, 10, and 12 \] Sustained virologic response (SVR, defined as plasma HCV RNA \< lower limit of quantification \[LLoQ\] at 24 weeks after treatment cessation) following antiviral treatment.
Secondary Outcome Measures: Safety and tolerability of therapy. \[ Time Frame: Up to 48 weeks \] measured by frequency of laboratory abnormalities , reported adverse events and discontinuations due to adverse events
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients with chronic HCV infection
Exclusion Criteria
* Co-infected Patients with HIV or Hepatitis B virus (HBsAg positive)
* hepatocellular carcinoma or other malignancies
* anticipated with difficulty of follow-up observation
1 Year
18 Years
ALL
No
Sponsors
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Beijing 302 Hospital
OTHER
Responsible Party
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Principal Investigators
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jin han, professor
Role: PRINCIPAL_INVESTIGATOR
Beijing 302 Hospital
Locations
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Beijing 302 Hospital
Beijing, Beijing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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beijing302-004
Identifier Type: -
Identifier Source: org_study_id
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