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临床试验/NCT03527316
NCT03527316已完成早期 1 期

Effect of MDMA (Serotonin Release) on Fear Extinction

University Hospital, Basel, Switzerland1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2019年10月18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
发起方
入组人数
30
试验地点
1
主要终点
Fear extinction measured by Fear-potentiated startle

研究概览

简要总结

Serotonin and oxytocin play a role in fear conditioning and fear extinction learning, psychological processes that are critically involved in psychiatric disorders such as posttraumatic stress disorder (PTSD). Specifically, administration of oxytocin has been shown to facilitate fear extinction in humans. Similarly, substances that release serotonin and oxytocin such as MDMA have been shown to enhance the extinction of fear memory in animals. However, there are no data on the effects of MDMA on fear extinction in humans. Therefore, the primary aim of this study is to investigate the role of acute serotonin release in the effects of fear extinction. MDMA will be used as pharmacological tool to induce serotonin release in this study.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Age between 18 and 50 years.
  • Understanding of the German language.
  • Understanding the procedures and the risks associated with the study.
  • Participants must be willing to adhere to the protocol and sign the consent form.
  • Participants must be willing to refrain from taking illicit psychoactive substances during the study.
  • Participants must be willing to drink only alcohol-free liquids and no coffee, black or green tea, or energy drink after midnight of the evening before the study session, as well as during the study day.
  • Participants must be willing not to drive a traffic vehicle or to operate machines within 48 h after substance administration.
  • Body mass index 18-29 kg/m2.

排除标准

  • Chronic or acute medical condition
  • Hypertension (>140/90 mmHg) or hypotension (SBP<85 mmHg)
  • Current or previous major psychiatric disorder
  • Psychotic disorder in first-degree relatives
  • Illicit substance use (with the exception of cannabis) of more than 5 times or any time within the previous month.
  • Participation in another clinical trial (currently or within the last 30 days)
  • Use of medications that may interfere with the effects of the study medications (any psychiatric medications)
  • Tobacco smoking (>10 cigarettes/day)
  • Consumption of alcoholic standard drinks (>10/week or >120 g ethanol/week)

研究组 & 干预措施

MDMA, Placebo

Experimental

Cross-over within-subjects design with both treatment conditions, separated by a wash-out phase

干预措施: MDMA (Drug)

MDMA, Placebo

Experimental

Cross-over within-subjects design with both treatment conditions, separated by a wash-out phase

干预措施: Placebo (Drug)

Placebo, MDMA

Experimental

Cross-over within-subjects design with both treatment conditions, separated by a wash-out phase

干预措施: MDMA (Drug)

Placebo, MDMA

Experimental

Cross-over within-subjects design with both treatment conditions, separated by a wash-out phase

干预措施: Placebo (Drug)

结局指标

主要结局

Fear extinction measured by Fear-potentiated startle

时间窗: 12 months

b) Fear-potentiated startle to conditioned stimuli

Fear extinction measured by Skin conductance response

时间窗: 12 months

a) Skin conductance response to conditioned stimuli

次要结局

  • Plasma concentration of Oxytocin(12 months)
  • Autonomic effects measured by Hearth rate(12 months)
  • Subjective effects measured by Visual analog scales(12 months)
  • Autonomic effects measured by Body temperature(12 months)
  • Plasma concentration of MDMA(12 months)
  • Autonomic effects measured by Blood pressure(12 months)
  • Subjective effects measured by State-trait anxiety inventory for state (STAI-S)(12 months)

研究者

发起方
University Hospital, Basel, Switzerland
申办方类型
Other
责任方
Sponsor

研究点 (1)

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