跳至主要内容
临床试验/NCT00123370
NCT00123370Unknown2 期

Randomised Placebo-Controlled Trial of Modafinil for Methamphetamine Dependence

The University of New South Wales4 个研究点 分布在 1 个国家目标入组 87 人开始时间: 2006年7月最近更新:
适应症
相关药物

试验速览

阶段
2 期
入组人数
87
试验地点
4
主要终点
Urinalysis results negative for methamphetamine over 10 weeks

研究概览

简要总结

The study aims to evaluate the safety and efficacy of modafinil (200 mg/day) over 10 weeks plus a tailored cognitive behavioural therapy program in the treatment of methamphetamine dependence.

详细描述

Modafinil is a novel wake promoting agent approved in Australia for the treatment of narcolepsy. Preliminary studies have suggested that modafinil may have value in the treatment of psychostimulant dependence through positive effects on mood, sleep patterns, concentration, fatigue and drug craving. It appears to be well tolerated with a low abuse potential. Sixty dependent methamphetamine users will be allocated to 2 equal groups. The experimental group will receive modafinil 200 mg/day for 10 weeks and a tailored cognitive behavioural therapy program. The control group will receive placebo under equivalent conditions. Primary outcome will be a between group comparison of methamphetamine negative urine samples over the 10 week study period. Adverse events, side effects, compliance, retention and self reported health, psychosocial and drug use will also be compared between the study groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Double

入排标准

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

入选标准

  • Diagnostic and Statistical Manual of Mental Disorders-Fourth Edition (DSM-IV) amphetamine dependence diagnosis
  • Amphetamine positive urine sample at intake
  • Regular current amphetamine use (2-3 days per week)
  • Aged 18 years or older

排除标准

  • Pregnant or nursing females
  • Hazardous concurrent uncontrolled physical or mental illness

结局指标

主要结局

Urinalysis results negative for methamphetamine over 10 weeks

时间窗: 10 weeks

Adverse events

时间窗: 10 weeks

Compliance

时间窗: 10 weeks

Retention

时间窗: 10 weeks

次要结局

  • Health outcomes(10 weeks)
  • Psychosocial outcomes(10 weeks)
  • Self reported drug use(10 weeks)

研究者

申办方类型
Other

研究点 (4)

Loading locations...

相似试验

Trial of Modafinil for Methamphetamine Dependence | 临床试验