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临床试验/NCT00736502
NCT00736502已完成不适用

Longterm Efficacy and Safety of NVP-based HAART in HIV-1 Positive Patients in the Daily Clinical Practice.

Boehringer Ingelheim17 个研究点 分布在 2 个国家目标入组 280 人开始时间: 2008年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
280
试验地点
17
主要终点
Proportion of Patients Reporting Adverse Events

研究概览

简要总结

The aim of this trial is to evaluate the safety and virological and immunological efficacy of Viramune® on a background of different antiretroviral drug combinations.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Proportion of Patients Reporting Adverse Events

时间窗: 48 weeks

the incidence of non serious adverse events and serious adverse events according to body system (= System Organ Class) and preferred term.

次要结局

  • Virologic Response (VR)(48 weeks)
  • Change in CD4+ Cell Count From Baseline to Week 48(Baseline and week 48)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (17)

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