NCT00867048已完成4 期
Strategic Timing of AntiRetroviral Treatment
适应症
干预措施
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 4,688
- 试验地点
- 218
- 主要终点
- Composite Endpoint of AIDS, Serious Non-AIDS Diagnoses, and All-cause Mortality
研究概览
简要总结
Objectives:
- To find out if the chance of developing a serious illness or of getting AIDS is less if patients start taking HIV medicines at a time when their cluster-of-differentiation-4 (CD4)+ cell count is still fairly high, instead of waiting until the CD4+ count is at the level where there is good evidence for starting medicines.
- To learn more about how a strategy of starting HIV medicines early might affect other aspects of care, such as the chances of developing other illnesses or resistance to HIV medicines, the frequency of doctor visits, the cost of medical care, and general health and satisfaction.
详细描述
Background:
- Most guidelines agree that if the number of your CD4+ cells (cells in your blood which help fight infection) drops below 350 cells/mm3, or if you have symptoms of AIDS, you should start taking HIV medicines. There are randomized trials that support this recommendation. (Randomized trials are usually considered the strongest form of evidence to support treatment decisions. Other studies, like observational studies, provide evidence too, but the evidence is often considered to be weaker than evidence from randomized trials. A randomized trial gives the most certain information about how well a treatment works because randomization makes sure each group is similar except for the treatment they receive.) Some experts believe that HIV treatment should be started even when the number of CD4+ cells is above 350 cells/mm3. For example, guidelines issued in the US in December 2009 include a new recommendation for starting HIV medicines if your CD4+ cell count is between 350 and 500 cells/mm3. However, this recommendation is based on information from observational studies, not randomized trials. We are doing this study to find out if the chances of getting a serious illness or of getting AIDS are less if people start taking HIV medicines at a time when their CD4+ cell counts are still fairly high, instead of waiting to take HIV medicines at a CD4+ count where there is good evidence for starting medicines.
Objectives:
- To find out if the chance of developing a serious illness or of getting AIDS is less if patients start taking HIV medicines at a time when their CD4+ cell count is still fairly high, instead of waiting until the CD4+ count is at the level where there is good evidence for starting medicines.
- To learn more about how a strategy of starting HIV medicines early might affect other aspects of care, such as the chances of developing other illnesses or resistance to HIV medicines, the frequency of doctor visits, the cost of medical care, and general health and satisfaction.
Eligibility:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
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
- 未提供
排除标准
- 未提供
研究组 & 干预措施
Early ART
Experimental
Initiate ART immediately following randomization
干预措施: All licensed antiretroviral medications (Drug)
Deferred ART
Active Comparator
Defer ART until the CD4+ count declines to <350 cells/cu mm or AIDS develops
干预措施: All licensed antiretroviral medications (Drug)
结局指标
主要结局
Composite Endpoint of AIDS, Serious Non-AIDS Diagnoses, and All-cause Mortality
时间窗: full follow-up, 9.3 years
次要结局
- AIDs or AIDs Related Death(full follow-up, 9.3 years)
- Death, All-cause Mortality(full follow-up, 9.3 years)
- Changes in Bone Mineral Density (in a Subset of Participants) Measure 1(4.5 years)
- Specific Non-AIDS Diagnoses(full follow-up, 9.3 years)
- Quality of Life- Mean Change From Baseline in a Visual Analog Scale (VAS) for Perceived Current Health(4.5 years)
- Large Artery Elasticity (in a Subset of Participants)(4.5 years)
- Transmission Risk Behavior Outcome 1(12 months)
- Changes in Bone Mineral Density (in a Subset of Participants) Measure 2(4.5 years)
- Change in Neurocognitive Function (in a Subset of Participants)(4.5 years)
- Transmission Risk Behavior Outcome 2(12 month visit)
- Small Artery Elasticity (in a Subset of Participants)(4.5 years)
- Rate of Lung Function Decline (in a Subset of Participants) Among(4.5 years)
- Rate of Lung Function Decline (in a Subset of Participants) Among Non-smokers(4.5 years)
研究者
研究点 (218)
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