NCT00135447已完成不适用
A Phase IV, Multicenter, Cross-sectional Study to Evaluate the I50L Substitution Among Subjects Experiencing Virologic Failure on a HAART Regimen Containing Atazanavir (ATV)
Bristol-Myers Squibb81 个研究点 分布在 1 个国家目标入组 5,000 人开始时间: 2004年9月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 5,000
- 试验地点
- 81
研究概览
简要总结
The purpose of this study is to find out the frequency of the I50L substitution among patients experiencing treatment failure on an atazanavir-containing regimen.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Atazanavir - containing antiretroviral regimen
- •Confirmed virologic failure defined as either:
- •HIV RNA by PCR greater than or equal to 1000 copies/mL after achieving a value of <400 copies/mL on at least 2 consecutive measurements or
- •HIV RNA greater than or equal to 1000 copies/mL after 24 weeks of continuous therapy
- •At least 18 years old
排除标准
- •Unable to give informed consent
- •Prisoners or subjects involuntarily incarcerated for treatment of psychiatric or physical illness
研究者
研究点 (81)
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