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临床试验/NCT00980408
NCT00980408已完成不适用

The NMDA Receptor Co-agonist D-cycloserine Accelerates Associative Learning in the Human Hippocampal CA Region

University Hospital, Bonn1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2008年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
120
试验地点
1
主要终点
fMRI during learning task

研究概览

简要总结

The hippocampus is particularly laden with n-methyl-d-aspartate (NMDA) receptors, and is at the same time one of the most important sites in declarative memory. The rationale of this study is that the NMDA partial agonist D-Cycloserine will promote learning compared to a placebo. On the other hand, the NMDA receptor antagonist Memantine might lead to reduced memory. We believe that the influence of NMDA receptors on memory can be determined via acute co-activation of the NMDA receptors with Cycloserine® (King Pharmaceuticals Ltd, active ingredient: DCycloserin, dose: 250 mg) and Memantine (Axura®, Merz, active ingredient: Memantine, dose: 20 mg)on both a behavioral and functional (fMRI) level.

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 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • German native language or native language level
  • Able to give written informed consent
  • right-handed

排除标准

  • inability to give written informed consent, underaged minors, contractually incapable persons, persons in legal custody
  • any psychiatric, neurological or internal illness
  • hematoporphyria (enzyme sickness)
  • intake of medication (except oral contraceptives)
  • simultaneous participation in other clinical studies
  • hypersensitivity to Memantine or other anti-dementia substances, or to D-Cycloserine
  • alcohol abuse
  • depression
  • serious anxiety or psychosis
  • serious kidney insufficiency
  • intake of Ethionamide or Isoniazide
  • pregnancy or women who are nursing
  • liver or kidney problems
  • intake of NMDA-antagonists, such as Amantadine, Ketamine, or Dextromethorphan
  • vegetarians
  • stomach ulcer, if treated with medication
  • renal tubular acidosis
  • urinary infections (with proteus bacteria)
  • recent heart attack, heart failure, or uncontrolled high blood pressure
  • intake of L-Dopa, dopaminergic agonists, and anticholinergics
  • intake of barbiturates, spasmolytics, Phenytoin, Amantadine, oral coagulators, warfarin, HCT (Hydrochlorothiazide)
  • heart or cranial operations
  • 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)
  • claustrophobia

研究组 & 干预措施

Sugar pill, behavioral glutamic acid

Placebo Comparator

Placebo condition for D-Cycloserine

干预措施: Sugar pill (Drug)

Sugar pill, fMRI, glutamic acid

Placebo Comparator

Placebo condition for D-Cycloserine, fMRI

干预措施: Sugar pill (Drug)

Sugar pill, memantine, behavioral

Placebo Comparator

Placebo condition Memantine, behavioral

干预措施: Sugar pill (Drug)

Sugar pill, memantine, fMRI

Placebo Comparator

Placebo condition Memantine, fMRI

干预措施: Sugar pill (Drug)

D-Cycloserine behavioral

Active Comparator

干预措施: Glutamic Acid (Drug)

D-Cycloserine, fMRI

Active Comparator

干预措施: Glutamic Acid (Drug)

Memantine, behavioral

Active Comparator

干预措施: Memantine (Drug)

Memantine, fMRI

Active Comparator

干预措施: Memantine (Drug)

结局指标

主要结局

fMRI during learning task

时间窗: once at drug administration

次要结局

未报告次要终点

研究者

发起方
University Hospital, Bonn
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rene Hurlemann

MD

University Hospital, Bonn

研究点 (1)

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