To determine the efficacy and safety of Peginterferón alfa-2a (40 KD) plus Ribavirin in patients who have relapsed or not responded to a previous suboptimal therapy based in Interferon.
An important number of co-infected patients were treated suboptimally in the past with others ineffective therapies interferon-based. All co-infected patients should be an opportunity of retreatment with actually therapies.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
PegInterferon 180 mcg/week, Adjusted body weight Ribavirin (1000 mg \<75 kg, 1200 mg \>75 kg)
Hospital Carlos III
Madrid, Madrid, Spain
% of patients with RNA-HCV undetectable
Time frame: 24 weeks after end of treatment
% of patients with RNA-HCV undetectable at different moments of the treatment according genotype, viremia, liver fibrosis, number of CD4 cells and previous therapy
Time frame: At weeks 4, 12, 24 and 48 on treatment
Ribavirin levels
Time frame: At weeks 4, 12, 24 and 48 on treatment
Impact of dose reduction peg-interferon and/or ribavirin
Time frame: At weeks 4, 12, 24 and 48 on treatment
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