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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01607021
Other study ID # beijing302-004
Secondary ID
Status Recruiting
Phase N/A
First received May 24, 2012
Last updated August 14, 2015
Start date April 2012
Est. completion date December 2015

Study information

Verified date August 2015
Source Beijing 302 Hospital
Contact rongrong wu
Phone +8610-63879589
Email wrr302@163.com
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational

Clinical Trial Summary

The aim of this study is to investigate the relationships between interleukin 28B genetic variants and the response to treatment of chronic hepatitis C in Chinese children.


Description:

Hepatitis C affects thousands of children throughout the world. Most children acquire the virus through vertical transmission, although parenteral routes of acquisition are also common. Affected children are usually asymptomatic and histological findings are mild with a low risk of progression, about 5% develop significant liver disease in childhood.

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 1 Year to 18 Years
Eligibility Inclusion Criteria:

- Aged 1-18 years

- Patients with chronic HCV infection

Exclusion Criteria:

- HCV infected patients previously treated with antiviral drugs

- Co-infected Patients with HIV or Hepatitis B virus (HBsAg positive)

- hepatocellular carcinoma or other malignancies

- anticipated with difficulty of follow-up observation

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Locations

Country Name City State
China Beijing 302 Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing 302 Hospital

Country where clinical trial is conducted

China, 

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