The purpose of this observational study is to compare two approved treatment regimen(s) containing boceprevir and telaprevir, as part of standard of care for the treatment of hepatitis C.
The objective of the study is to compare the effect of adding 2 oral hepatitis C virus (HCV) protease inhibitors, telaprevir versus boceprevir, as part of current standard treatment regimen with (pegylated-interferon-alpha + ribavirin) for HCV Genotype-1 infection. Data will be obtained from medical records of consenting patients.
Study Type
OBSERVATIONAL
Enrollment
37
Southern Illinois University School of Medicine
Springfield, Illinois, United States
Virologic Response
Sustained Virologic Response (SVR) rates will be compared between the two arms of treatment through measured HCV RNA levels after 24 weeks, 48 weeks and 96 weeks after completion of treatment.
Time frame: up to 96 weeks post treatment
Adverse events
Comparison of rates and severity of adverse events between the two study arms
Time frame: 24, 48, and 96 weeks post treatment
Effect of baseline variables on treatment outcome
Analyze the effects of baseline variables on treatment outcome between the two groups- age, race, social economic status.
Time frame: 24, 48, and 96 weeks post treatment
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.