Primary objective is to measure sustained viral response given to continuation or prolongation of combined Pegasys\&Copegus treatment Secondary objective is to measure histological response given to continuation or prolongation of combined Pegasys\&Copegus treatment measured by non-invasive methods
Prospective, multicentre, randomized, open-label comparative study According to our national guideline of management of patient with chronic viral hepatitis, patients need to stop therapy if they do not achieve response. These patients can enter to the study at two time points: * at week 16, if HCV RNS PCR measured at week 12 is positive and serum ALT \> 1ULN, but decreased * at week 28, if HCV RNS PCR measured at week 24 is still positive, but serum ALT \< 2ULN. Patients are randomized to one of the following arms: * S (standard) group: Pegasys\&Copegus combined therapy 180 mcg/week \& weight/based 1000-1200 mg/day for a total of 48 weeks of treatment * P (prolonged) group: Pegasys\&Copegus combined therapy 180 mcg/week \& -weight/based 1000-1200 mg/day for a total of 72 weeks of treatment. After completing treatment period patients enter into a 24-week follow up.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Szt. László Hospital
Budapest, Hungary
RECRUITINGSustained viral response given to continuation or prolongation of combined Pegasys&Copegus treatment
Histological response given to continuation or prolongation of combined Pegasys&Copegus treatment measured by non-invasive methods
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