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临床试验/NCT00033072
NCT00033072Unknown1 期

Assessment of Potential Interactions Between Intravenous Methamphetamine and Oral Selegiline

National Institute on Drug Abuse (NIDA)2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2001年9月最近更新:
适应症
相关药物

试验速览

阶段
1 期
入组人数
16
试验地点
2
主要终点
pharmacokinetic assessment

研究概览

简要总结

The purpose of this study is to assess the potential interactions between intravenous methamphetamine and oral selegiline.

详细描述

To determine the safety of the selegiline concurrent with d-methamphetamine challenges of 15mg & 30mg i.v. with the focus being on cardiovascular responses (HR,BP) to the i.v. methamphetamine challenges. This is a randomized, single-blind, placebo-controlled, two-arm study design to evaluate the safety of selegiline treatment, compared to placebo treatment, concurrent with i.v. methamphetamine challenges.

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Treatment
盲法
Single

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Volunteers who meet DSM-4 criteria for methamphetamine abuse or dependence; non-treatment seeking individuals
  • Be able to verbalize understanding of consent form; provide written informed consent

排除标准

  • Please contact site for more information

结局指标

主要结局

pharmacokinetic assessment

safety of selegiline

次要结局

未报告次要终点

研究者

申办方类型
Nih

研究点 (2)

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