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Influence of Nevirapine on HCV Viral Load

Not Applicable
Conditions
HCV Infection.
HCV Viral Load.
Interventions
Registration Number
NCT01277627
Lead Sponsor
Valme University Hospital
Brief Summary

Nevirapine-based antiretroviral therapy is associated with lower plasma HCV viral load in HIV/HCV-coinfected individuals.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
60
Inclusion Criteria
  • HIV infection.
  • Older than 18 years.
  • Chronic hepatitis C.
  • Undetectable HIV viral load during one year before starting study.
  • To have not received HCV therapy during one year before starting study.
  • To have not started efavirenz or protease inhibitors o nucleoside analogs during 6 months before starting study.
  • Non contraindications for drugs included in this study.
  • To change an antiretroviral regimen including efavirenz or protease inhibitors by nevirapine due to side effects, interactions or pregnancy (NVP group)
  • To continue with a antiretroviral regimen including efavirenz or protease inhibitors (non-NVP group)

Both groups will be matched according to these variables:

  • Liver stiffness.
  • HCV genotype.
  • Hospital.
  • Time from starting antiretroviral therapy.
  • Previous third drug (EFV or PI) to introduction of NVP.
Exclusion Criteria
  • HCV therapy during follow-up

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Nevirapineefavirenz, protease inhibitors-
Non-nevirapineNevirapine-
Non-nevirapineefavirenz, protease inhibitors-
NevirapineNevirapine-
Primary Outcome Measures
NameTimeMethod
Changes in HCV viral load48 weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Valme University Hospital

🇪🇸

Seville, Spain

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