A Study of HIV in Newly Infected Individuals
Infected Participants Protocol: Evaluation of Natural History of HIV Infection in Newly HIV-Infected Persons in HIVNET Target Populations
The purpose of this study is to see how HIV reacts in the immune systems of patients who have recently been infected with HIV. This study also examines HIV's resistance to anti-HIV drugs in newly infected patients.
Certain populations are good candidates for participation in HIV vaccine trials. These groups include men who have sex with men, IV drug users, and women at risk of getting HIV through heterosexual contact. Learning how HIV behaves in these populations once they become infected can help with the planning of future HIV vaccine studies.
研究概览
地位
条件
详细说明
This study provides an opportunity to prospectively monitor markers of HIV infection and disease progression in cohorts suitable for HIV vaccine trials. The detection of changes in HIV phenotype and genotype, clinical progression rates, and antiretroviral resistance within study populations over time are important for planning future HIV vaccine trials.
This study consists of two parts. Part A includes HIV-infected patients who enrolled in HIVNET D01.1 (infected-participants cohort of HIVNET D01) and whose HIV disease has been closely monitored and characterized. This study continues to monitor these patients with follow-up evaluations every 3 months for the first 18 months and then every 6 months thereafter. Part B includes newly HIV-infected patients. These patients are monitored with clinical and laboratory evaluations at 0, 1, 3, 6, 9, 12, and 18 months, and then every 6 months through Year 5.
研究类型
联系人和位置
学习地点
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California
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Los Angeles、California、美国、90033
- Los Angeles County / Health Research Assoc / Drew Med Ctr
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San Francisco、California、美国、94102
- San Francisco Dept of Hlth / AIDS Office
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Colorado
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Denver、Colorado、美国、80204
- Denver Dept of Public Health / HIVNET
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Illinois
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Chicago、Illinois、美国、60612
- Univ of Illinois Chicago / Howard Brown Hlth Ctr
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Maryland
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Baltimore、Maryland、美国、21205
- Johns Hopkins Univ
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Massachusetts
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Boston、Massachusetts、美国、02115
- Fenway Community Health Ctr / HIVNET
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New York
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Bronx、New York、美国、10453
- Bronx-Lebanon Hosp Ctr
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Bronx、New York、美国、10456
- New York Blood Ctr
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New York、New York、美国、10016
- New York Univ Med Ctr
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Pennsylvania
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Philadelphia、Pennsylvania、美国、19104
- Univ of Pennsylvania / HIVNET
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Rhode Island
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Providence、Rhode Island、美国、02906
- Miriam Hosp
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Washington
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Seattle、Washington、美国、98104
- Univ of Washington
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
描述
Inclusion Criteria
Patients must have:
- HIV infection, as documented by enrollment in HIVNET D01.1 (Part A patients) or by standard HIV serological tests or demonstrated HIV infection on virologic assay (Part B patients).
Part A only:
- Previous enrollment in infected-participants cohort of HIVNET D01.
Part B only:
- Initial HIV-seronegativity on an HIVNET protocol (other than an HIV vaccine protocol) and testing positive for HIV at a subsequent clinic visit.
- Confirmation of HIV infection and documentation of HIV negative antibody test within 8 months of first positive test.
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions are excluded:
- An obvious psychological/psychiatric disorder that would invalidate the informed consent process or otherwise contraindicate participation in the study.
Prior Medication:
Excluded:
- Participation in a HIVNET HIV vaccine trial.
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
|---|
|
A
HIV-infected individuals enrolled in HIVNET D01
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B
Individuals with newly acquired HIV infection
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Detection of changes in HIV phenotype and genotype
大体时间:Throughout study
|
Throughout study
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Clinical progression rates
大体时间:Throughout study
|
Throughout study
|
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Antiviral resistance
大体时间:Throughout study
|
Throughout study
|
合作者和调查者
调查人员
- 学习椅:Celum C
- 学习椅:Buchbinder S
- 学习椅:Sheppard H
研究记录日期
研究主要日期
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.