跳至主要内容
临床试验/NCT01277627
NCT01277627Unknown不适用

Influence of Nevirapine on HCV Viral Load Among HIV/HCV-coinfected Patients

Valme University Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2011年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
1
主要终点
Changes in HCV viral load

研究概览

简要总结

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

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • HCV therapy during follow-up

研究组 & 干预措施

Nevirapine

Active Comparator

干预措施: Nevirapine (Drug)

Nevirapine

Active Comparator

干预措施: efavirenz, protease inhibitors (Drug)

Non-nevirapine

Active Comparator

干预措施: Nevirapine (Drug)

Non-nevirapine

Active Comparator

干预措施: efavirenz, protease inhibitors (Drug)

结局指标

主要结局

Changes in HCV viral load

时间窗: 48 weeks

次要结局

未报告次要终点

研究者

发起方
Valme University Hospital
申办方类型
Other

研究点 (1)

Loading locations...

相似试验