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临床试验/NCT00476606
NCT00476606已完成不适用

Treatment Outcome of Children With HIV Infection

The HIV Netherlands Australia Thailand Research Collaboration3 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2003年3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
状态
已完成
入组人数
500
试验地点
3
主要终点
1. To collect clinical and immunologic data of children treated with HAART 2. To collect clinical outcome data on children with HIV infection 3. To provide the best possible care to children with HIV infection

研究概览

简要总结

To evaluate clinical and immunological outcome of children treated with HAART.

详细描述

This is a long term cohort study that was started in 2002. Currently, there are 120 children enrolled in the study and are receiving HIV care according to standard practice set by the Thai Ministry of Public Health. HIV-infected parents also receive care at the same clinic.

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
1 Day 至 20 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Children who are part of the ATC program at Chulalongkorn hospital and at HIV-NAT, The Thai Red Cross AIDS research center
  • Children who fulfil criteria to start HAART according to the ATC program
  • Children who are switched to second regimen or salvage therapy
  • Children who are on any antiretroviral regimens, including post trial children from other HIV-NAT study (both at HIV-NAT and Khon Kaen University sites)
  • Children with HIV infection who are not on antiretroviral therapy
  • Caretakers understand the purpose of data and plasma samples collection, and have signed the consent form

排除标准

  • Patients and caretakers may choose to stop HAART at anytime during the study. If they agree, we would continue to follow them in this study.

研究组 & 干预措施

Long-term pediatric cohort

Long-term follow-up cohort since 2003

干预措施: Zidovudine, Stavudine, Didanosine, Lamivudine (Drug)

Long-term pediatric cohort

Long-term follow-up cohort since 2003

干预措施: Nevirapine, Efavirenz (Drug)

Long-term pediatric cohort

Long-term follow-up cohort since 2003

干预措施: LPV/r, Saquinavir, Indinavir, Ritonavir, Nelfinavir (Drug)

结局指标

主要结局

1. To collect clinical and immunologic data of children treated with HAART 2. To collect clinical outcome data on children with HIV infection 3. To provide the best possible care to children with HIV infection

时间窗: every 3 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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