临床试验/ACTRN12612001194853

ACTRN12612001194853已完成3 期

The CNS sub-study of a randomised, double-blind, placebo-controlled, clinical trial to compare the safety and efficacy of reduced dose efavirenz (EFV) with standard dose EFV plus 2N(t)RTI in antiretroviral-naive HIV-infected individuals over 96 weeks

Kirby Institute, University of New South Wales0 个研究点目标入组 40 人开始时间: 2012年11月13日最近更新: 2020年1月13日

试验速览

阶段: 3 期
状态: 已完成
发起方
入组人数: 40

研究概览研究设计入排标准研究者记录与标识符相似试验

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: Randomised controlled trial
主要目的: Treatment
盲法: Blinded (masking used)

入排标准

年龄范围: 16 Years 至 o limit（—）
性别: All

入选标准

•All subjects entering into the main study protocol at participating centres will be eligible to enter this sub-study

排除标准

•Existing neurological disease which in the opinion of the
•investigator would be a contra-indication to lumbar
•puncture examination
•CNS opportunistic infections in the past 12 weeks
•Bacterial or viral meningitis in the past 12 weeks
•Head injury requiring medical assessment in the past 12 weeks

研究者

发起方

Kirby Institute, University of New South Wales

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