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临床试验/NCT00002246
NCT00002246已完成3 期

A Pilot Open Label, Multicenter Study to Evaluate the Role of Stavudine (d4T) in the Treatment of AIDS Dementia Complex

Bristol-Myers Squibb5 个研究点 分布在 3 个国家目标入组 20 人开始时间: 1997年10月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
20
试验地点
5

研究概览

简要总结

The purpose of this study is to see if adding stavudine (d4T) to anti-HIV drug regimens (with or without zidovudine, ZDV) can improve symptoms of AIDS Dementia Complex (ADC, problems involving the brain or spinal cord) in HIV-positive patients.

详细描述

In this open-label, multicenter, multinational study, ZDV is replaced with d4T in ZDV-containing regimens, or d4T is added to non-ZDV-containing regimens in 20 patients experiencing ADC. Patients are defined as having failed treatment if they progress by one ADC stage on the MSK (Memorial Sloan Kettering) rating scale on study (i.e., from Stage 1 to 2 or Stage 2 to 3). Patients are evaluated on a weekly basis until the dementia deterioration is confirmed to be caused by HIV-1. The effect of d4T-containing regimens is assessed for the following parameters: neurological status, survival, AIDS-defining conditions, CSF (cerebrospinal fluid) and plasma viral load, CSF and blood immunological markers, blood CD4 cell counts, and viral resistance. This study also assesses the pharmacokinetics of d4T in the CSF and in the blood.

研究设计

研究类型
Interventional
主要目的
Treatment

入排标准

年龄范围
13 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •You may be eligible for this study if you:
  • •Are HIV-positive.
  • •Are at least 13 years old (need consent if under 18).
  • •Have AIDS Dementia Complex.
  • •Have been on a stable anti-HIV drug regimen for at least 8 weeks prior to study entry.
  • •Agree to use effective methods of birth control during the study.
  • •Are available for at least 16 weeks of study.

排除标准

  • •You will not be eligible for this study if you:
  • •Have ever taken d4T.
  • •Have a neurological (brain/spinal cord) disease, such as chronic seizures or head injury, or certain other conditions that would interfere with your ability to complete the study.
  • •Are pregnant or breast-feeding.
  • •Abuse alcohol or drugs.
  • •Have peripheral neuropathy or a newly diagnosed AIDS-defining infection that requires treatment at the time of study enrollment.
  • •Have received certain medications.
  • •Cannot take medications by mouth.
  • •Have severe diarrhea for at least 7 days in a row within 30 days prior to study entry.

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry

研究点 (5)

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