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临床试验/NCT00845013
NCT00845013已完成不适用

Epidemiology and Pathogenesis of HIV-Associated Pulmonary Hypertension

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 365 人开始时间: 2007年11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
365
试验地点
1
主要终点
pulmonary artery pressure

研究概览

简要总结

The purpose of this study is to describe the epidemiology of pulmonary hypertension in individuals with HIV infection and to investigate its pathogenesis. We propose to conduct a prospective observational cohort study to determine the association between highly active antiretroviral therapy (HAART) and viral suppression in HIV-infected patients who have been identified to have pre-clinical pulmonary hypertension (Aim 1). In addition, we will investigate the mechanistic role of the HIV-1 Nef protein and HHV-8 infection in the development and progression of pulmonary hypertension in individuals with HIV (Aim 2). We will also investigate endothelial function in HIV-infected patients with pulmonary hypertension (Aim 3).

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

  • Infection with HIV greater than 6 months in duration
  • Right heart catheterization showing PASP > 30mm Hg
  • Ability to provide reliable history of HIV medications or has received the majority of medical care from San Francisco General Hospital with available records of medical treatment.
  • Ability to participate in follow-up for the duration of the study.

排除标准

  • Known significant cardiovascular disease, including clinically significant valvular heart disease, congenital heart disease, current or prior symptomatic coronary disease, or known cardiomyopathy.
  • Any known pulmonary disease that could potentially cause pulmonary hypertension.
  • A pO2 by pulse oximetry below 90% on room air.
  • Obstructive sleep apnea.
  • Known collagen vascular disease.
  • History of anorexigen use
  • Age less than 18 years old.
  • Other co-morbidities for which the investigators, in conjunction with the primary care provider, believe render the participant with an expected survival of 6 months or less.

结局指标

主要结局

pulmonary artery pressure

时间窗: 3 years

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 (1)

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