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临床试验/ACTRN12607000247471
ACTRN12607000247471已完成不适用

A Study of the Effect of Probenecid on the Pharmacokinetics and Pharmacodynamics of Allopurinol at Steady-State in Patients with Gout

Department of Clinical Pharmacology and Toxicology, St Vincent’s Hospital Sydney Ltd0 个研究点目标入组 50 人开始时间: 2007年5月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Patients taking allopurinol for the indication of hyperuricaemia and/or gout.

排除标准

  • 1. A history of sensitivity to allopurinol or probenecid2. A history of nephrolithiasis3. Patients taking drugs likely to interfere with the pharmacokinetics of allopurinol or probenecid including: salicylates (high doses) 4. Drugs likely to interact with probenecid including: valaciclovir, acyclovir, famiciclovir, penciclovir, ganciclovir, zidovudine, methotrexate, lorazepam, midazolam, nitrazepam. Note: Drugs which may affect plasma urate concentrations need to be taken consistently throughout the study to avoid biasing the plasma urate concentrations.

研究者

发起方
Department of Clinical Pharmacology and Toxicology, St Vincent’s Hospital Sydney Ltd

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