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临床试验/NCT00000670
NCT00000670已完成不适用

Safety and Tolerance of Zidovudine With Probenecid and the Effect of Probenecid on Zidovudine Pharmacokinetics Over Four Weeks

National Institute of Allergy and Infectious Diseases (NIAID)2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2001年8月31日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
2

研究概览

简要总结

To evaluate the interaction of probenecid with zidovudine (AZT). Because AZT is eliminated quickly from the body, it must be taken frequently. A previous study showed that probenecid slowed the elimination of AZT without side effects, but that study lasted only 5 days. This study is to see whether this effect continues for 1 month and whether the continuation of probenecid and AZT is free of side effects over 1 month.

详细描述

Because AZT is eliminated quickly from the body, it must be taken frequently. A previous study showed that probenecid slowed the elimination of AZT without side effects, but that study lasted only 5 days. This study is to see whether this effect continues for 1 month and whether the continuation of probenecid and AZT is free of side effects over 1 month.

Patients are hospitalized overnight on three separate occasions. On the first admission, AZT is administered every 4 hours. On the second day, 15 blood samples are taken to determine how fast the AZT enters and is removed from the bloodstream (pharmacokinetics). On the second day, after all the blood specimens have been collected, patient starts taking probenecid by mouth every 8 hours, and is discharged from the research unit. The AZT dose is then taken every 8 hours. One week later and again 3 weeks after that, patient is readmitted overnight and the blood sampling to measure AZT levels is repeated. AMENDED: 8 additional patients will be enrolled using the same doses of AZT but a lower dose of probenecid.

研究设计

研究类型
Interventional
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

  • •Concurrent Medication:
  • •Interferon.
  • •Aerosolized pentamidine for Pneumocystis carinii pneumonia (PCP) prophylaxis.
  • •Concurrent Treatment:
  • •Radiation for skin lesions.
  • •Patients with symptomatic HIV infection taking zidovudine (AZT) five or six times a day as therapy. Includes patients with AIDS who have history of cytologically confirmed Pneumocystis carinii pneumonia (PCP), patients with advanced AIDS related complex (ARC), and HIV antibody positive patients.
  • •Patients must be able to give written informed consent.

排除标准

  • •Co-existing Condition:
  • •Patients with the following are excluded:
  • •Allergy to probenecid.
  • •Any underlying medical condition sufficient, in the investigator's opinion, to prevent adequate compliance with study therapy.
  • •History of urinary tract urate stones or gout.
  • •Becoming acutely ill, unstable, or febrile.
  • •Concurrent Medication:
  • •Methotrexate.
  • •Antiretroviral drugs.
  • •Ganciclovir.
  • •Amphotericin.
  • •Experimental drugs.
  • •Isoniazid.
  • •Pyrazinamide.
  • •Flucytosine.
  • •Intravenous pentamidine.
  • •Fansidar.
  • •Antineoplastic drugs not specifically allowed.
  • •Trimethoprim / sulfamethoxazole.
  • •Valproic acid.
  • •Rifampin.
  • •Sulfonylureas.
  • •Concurrent Treatment:
  • •Radiation not specifically allowed.
  • •Patients with the following are excluded:
  • •Allergy to probenecid.
  • •Any underlying medical condition sufficient, in investigator's opinion, to prevent adequate compliance with study therapy.
  • •History of urinary tract urate stones or gout.
  • •Becoming acutely ill, unstable, or febrile.

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (2)

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