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临床试验/NCT00630097
NCT00630097Unknown2 期

A Dose Ranging Study of Modafinil for Methamphetamine Dependence

California Pacific Medical Center Research Institute2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2009年12月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
入组人数
90
试验地点
2
主要终点
Methamphetamine-negative urine samples will be analyzed using a generalized estimating equation model

研究概览

简要总结

Patients treated for methamphetamine dependence have high rates of relapse, and no pharmacotherapy has yet been demonstrated to be efficacious. Modafinil (d, l-2-[(diphenylmethyl)sulfinyl]acetamide) is a novel wake- and vigilance-promoting agent that is chemically and pharmacologically dissimilar to CNS stimulants. It is well tolerated and has low abuse liability compared to CNS stimulants. Modafinil is FDA approved for a variety of sleep disorders, may relieve methamphetamine withdrawal symptoms, improves cognitive function, has been shown to reduce cocaine use in dependent users, and is safe when coadministered with intravenous methamphetamine. We will conduct a randomized dose ranging clinical trial of modafinil to establish its safety and efficacy as a pharmacotherapy for methamphetamine dependence.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 50 years
  • Patient is agreeable to conditions of study and signs consent form

排除标准

  • 未提供

结局指标

主要结局

Methamphetamine-negative urine samples will be analyzed using a generalized estimating equation model

时间窗: end of study

次要结局

未报告次要终点

研究者

研究点 (2)

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