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临床试验/NCT01512316
NCT01512316撤回不适用

The Effect of D-cycloserine on Fear Learning and Extinction

Universitaire Ziekenhuizen KU Leuven1 个研究点 分布在 1 个国家开始时间: 2012年1月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
change in BOLD-signal during a fear conditioning task

研究概览

简要总结

The present study investigates the effect of d-cycloserine on learning and unlearning of fear in healthy humans and its underlying effect on the amygdala.

As a second objective, the effect of genotype on fear learning will be studied.

详细描述

A growing body of evidence suggests that the extinction of fear is mediated by the N-methyl-D-aspartate (NMDA) receptor activity in the basolateral amygdala. Intra-amygdala infusions of antagonists of this glutamate receptor in small animals (eg: rats, mice) have demonstrated a blockage of fear acquisition and extinction. Agonists, on the other hand, facilitate conditioned fear extinction.

The animal studies are all based on the simple fear learning paradigm of conditioning. However, it is not clear that human anxiety disorders are based on prior conditioning encounter. Therefore it is important to disentangle the effect of DCS on acquisition and extinction in the context of a simple learning paradigm, particular its effect on the human amygdala.

研究设计

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

入排标准

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

入选标准

  • No axis I diagnosis compatible with the DSM-IV by means of a structured diagnostic interview
  • Right-handed

排除标准

  • Current psychopharmacological or psychological treatment.
  • The presence of a physical/medical condition that may interfere with the study.
  • A contraindication for the use of DCS
  • Pacemaker, medication pump (such as insulin pump), hearing aid, removable prosthodontics
  • Metal in or on body (such as acupuncture needles, artificial limbs, stents, metal splints, clips, implanted electrodes, tattoos, or piercings)

研究组 & 干预措施

d-Cycloserine Acquisition

Active Comparator

d-Cycloserine will be given on day1, before acquisition

干预措施: d-Cycloserine (Drug)

d-Cycloserine Acquisition

Active Comparator

d-Cycloserine will be given on day1, before acquisition

干预措施: Saliva sample (Genetic)

d-Cycloserine Acquisition

Active Comparator

d-Cycloserine will be given on day1, before acquisition

干预措施: Functional neuroimaging (fMRI) (Other)

d-Cycloserine Extinction

Active Comparator

d-Cycloserine will be administered on day2, before extinction

干预措施: d-Cycloserine (Drug)

d-Cycloserine Extinction

Active Comparator

d-Cycloserine will be administered on day2, before extinction

干预措施: Saliva sample (Genetic)

d-Cycloserine Extinction

Active Comparator

d-Cycloserine will be administered on day2, before extinction

干预措施: Functional neuroimaging (fMRI) (Other)

Placebo

Placebo Comparator

A placebo pill will be administered on day1 and 2

干预措施: Lactose pill (Drug)

Placebo

Placebo Comparator

A placebo pill will be administered on day1 and 2

干预措施: Saliva sample (Genetic)

Placebo

Placebo Comparator

A placebo pill will be administered on day1 and 2

干预措施: Functional neuroimaging (fMRI) (Other)

结局指标

主要结局

change in BOLD-signal during a fear conditioning task

时间窗: t0, t+24, t+48

Subjects will participate in a 3-day experiment. Day1 (t0): Acquisition Day2 (T+24): extinction Day3 (T+48): re-exposure

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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