chronic hepatitis C
Conditions
Interventions
None listed
Sponsors
Hiroshima University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: genotype 2 HCV-infected patients
Exclusion criteria
Exclusion criteria: Patients with decompensated cirrhosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| sustained virological response (negative for serum HCV RNA at 24 weeks after the treatment) | — |
Secondary
| Measure | Time frame |
|---|---|
| Hemoglobin during the treatment period | — |
Countries
Japan
Contacts
Public ContactMichio Imamura
Applied Life Science, Institute of Biomedical & Health Science, Hir oshima University Department of Gastroenterology a nd Metabolism
Outcome results
None listed