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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00723242
Other study ID # unknown
Secondary ID
Status Completed
Phase N/A
First received July 24, 2008
Last updated July 24, 2008
Start date April 2002
Est. completion date December 2004

Study information

Verified date July 2008
Source University College, London
Contact n/a
Is FDA regulated No
Health authority United Kingdom: National Health Service
Study type Interventional

Clinical Trial Summary

The role of the dendritic cells, the most potent antigen presenting cells, in the establishment of chronic hepatitis C is not established. The study aims to define whether the dendritic cells are affected by the hepatitis C virus and whether that bears an impact on the antiviral immune response they generate. The hypothesis is explored by investigating a group of patients prior to and after the initiation of standard treatment for hepatitis C with pegylated Interferon and Ribavirin.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date December 2004
Est. primary completion date December 2004
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- anti-HCV positive

- HCV RNA positive

Exclusion Criteria:

- contraindications for antiviral treatment

- concurrent chronic viral infections

Study Design

Primary Purpose: Basic Science


Intervention

Drug:
Viraferon-peg and Rebetol


Locations

Country Name City State
United Kingdom University College Hospital London

Sponsors (2)

Lead Sponsor Collaborator
University College, London Schering-Plough

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Basic science research (immunology of hepatitis C)in hepatitis c patients receiving established, standard antiviral treatment (pegylated Interferon+Ribavirin) No
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