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临床试验/NCT03790618
NCT03790618已完成1 期

Effect of Stimulant Drugs on Social Perception

University of Chicago1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2016年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
36
试验地点
1
主要终点
Responses to Affective Touch

研究概览

简要总结

The study will improve our understanding of the "prosocial" effects of ± 3,4-Methylenedioxymethamphetamine (MDMA), relative to a prototypical stimulant, methamphetamine (MA). The investigators seek to characterize the "uniquely social" effects of MDMA.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • High school degree
  • English fluency
  • Has used MDMA

排除标准

  • Pregnant or trying to become pregnant
  • Any medical or psychiatry condition

研究组 & 干预措施

High dose MDMA

Experimental

Subjects will attend one session during which they will receive 1.5mg/kg MDMA.

干预措施: 3,4-Methylenedioxymethamphetamine (Drug)

Placebo

Placebo Comparator

Subjects will attend one session during which they will receive a placebo capsule.

干预措施: 3,4-Methylenedioxymethamphetamine (Drug)

Placebo

Placebo Comparator

Subjects will attend one session during which they will receive a placebo capsule.

干预措施: methamphetamine (Drug)

Low dose MDMA

Experimental

Subjects will attend one session during which they will receive 0.75mg/kg MDMA.

干预措施: 3,4-Methylenedioxymethamphetamine (Drug)

Low dose MDMA

Experimental

Subjects will attend one session during which they will receive 0.75mg/kg MDMA.

干预措施: methamphetamine (Drug)

High dose MDMA

Experimental

Subjects will attend one session during which they will receive 1.5mg/kg MDMA.

干预措施: methamphetamine (Drug)

Methamphetamine

Experimental

Subjects will attend one session during which they will receive 20mg methamphetamine.

干预措施: 3,4-Methylenedioxymethamphetamine (Drug)

Methamphetamine

Experimental

Subjects will attend one session during which they will receive 20mg methamphetamine.

干预措施: methamphetamine (Drug)

结局指标

主要结局

Responses to Affective Touch

时间窗: End of study (time 0 and approximately six weeks later)

Participants will complete an affective touch task during which time they will rate pleasantness of touch on a likert scale of 1-7, with higher scores indicating greater ratings of pleasantness

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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