Hepatitis C, Chronic
Conditions
Brief summary
The purpose of this study is to evaluate the efficacy and safety of low-dose interferon-alfa-2b plus ribavirin compared to the standard-dose of the same combination in patients with chronic hepatitis C.
Interventions
Sponsors
Kyoto University
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Clinical diagnosis of Chronic Hepatitis C. Must be infected with genotype 1b viruses
Exclusion criteria
* Hemoglobin levels\<8.5g/dL, * Platelet counts\<50,000/mm3, * Total polymorphonuclear counts\<1000/mm3 * Pregnancy, * Renal dysfunction,
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| rate of sustained viral response | 6 months |
Countries
Japan
Outcome results
None listed