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临床试验/NCT04053036
NCT04053036已完成早期 1 期

Effects of MDMA on Responses to Affective Touch in Individuals With a Range of Autistic Traits

University of Chicago1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2019年8月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
入组人数
22
试验地点
1
主要终点
Change in Responses to Affective Touch

研究概览

简要总结

To study the effects of a psychostimulant on responses to affective touch in individuals with a range of autistic traits

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • BMI between 19 and 30 (no one under 130 lbs)
  • Smokers smoking less than 25 cigarettes per week
  • Have used ecstasy no more than 40 times with no adverse responses.

排除标准

  • High blood pressure
  • Any medical condition requiring regular medication
  • Individuals with a current (within the last year) DSM-IV Axis 1 diagnosis
  • Individuals with a history of dependence on stimulant drugs.
  • Women who are pregnant or trying to become pregnant

研究组 & 干预措施

Placebo Then MDMA

Experimental

Participants first receive placebo at their first session in the laboratory. Then will return to the laboratory 72 hours later and will receive MDMA (1.5 mg/kg)

干预措施: MDMA (Drug)

Placebo Then MDMA

Experimental

Participants first receive placebo at their first session in the laboratory. Then will return to the laboratory 72 hours later and will receive MDMA (1.5 mg/kg)

干预措施: Placebo oral tablet (Drug)

MDMA Then Placebo

Experimental

Participants first receive MDMA (1.5 mg/kg) at their first session in the laboratory. Then will return to the laboratory 72 hours later and will receive placebo.

干预措施: MDMA (Drug)

MDMA Then Placebo

Experimental

Participants first receive MDMA (1.5 mg/kg) at their first session in the laboratory. Then will return to the laboratory 72 hours later and will receive placebo.

干预措施: Placebo oral tablet (Drug)

结局指标

主要结局

Change in Responses to Affective Touch

时间窗: 1.5 hrs after drug or placebo administration.

Participants will complete an affective touch task during which time they will rate pleasantness of touch on a scale of -10 to +10 using an analog scale. Higher ratings indicate greater 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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