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临床试验/NCT00215878
NCT00215878已完成2 期

D-serine for Posttraumatic Stress Disorder Treatment

Herzog Hospital1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2003年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
22
试验地点
1
主要终点
CAPS scores

研究概览

简要总结

The aim of this study is to asses the effects of the NMDA receptor full agonist D-serine while used as adjuvant treatment for individuals suffering from chronic posttraumatic stress disorder (PTSD). Dysfunction of neurotransmission mediated at NMDA receptor plays a cardinal role in the pathophysiology of PTSD and PTSD patients typically suffer from cognitive dysfunctions and avoidance& depressive symptomatology that may be mediated by NMDA receptor function deficits.

Thus, enhancement of NMDA activity by using D-serine may be beneficial in the treatment of PTSD. The study design involves two 6 week periods during which the participants will be randomly assigned to receive treatment with D-serine (~2g /dy)and placebo. This design allows each participant the opportunity to respond to the experimental treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
25 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Chronic PTSD (DSM-IV diagnosis)

排除标准

  • Other psychiatric diagnosis
  • Substance abuse
  • Unstable medical condition

研究组 & 干预措施

1

Placebo Comparator

Adjuvant 6 weeks treatment with placebo (~2g /day)

干预措施: D-serine (~2g /day) (Drug)

2

Experimental

Adjuvant 6 weeks treatment with D-serine (~2g /day)

干预措施: D-serine (~2g /day) (Drug)

结局指标

主要结局

CAPS scores

时间窗: 6 week treatment

次要结局

未报告次要终点

研究者

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

Heresco-Levi Uriel

Principal Investigator

Herzog Hospital

研究点 (1)

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