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临床试验/ISRCTN89039808
ISRCTN89039808已完成2 期

Efficacy and safety of three doses of S 38093 (2, 5 and 20 mg/day) versus placebo in patients with mild to moderate Alzheimer's disease

Institut de Recherches Internationales Servier (France)0 个研究点目标入组 711 人开始时间: 2011年7月28日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
711

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • •1. Age 55-85 years
  • •2. School education more than or equal to 4 years
  • •3. Able to perform neuropsychological tests
  • •4. Have adequate visual and auditory acuity with the usual corrective aids to allow neuropsychological testing
  • •5. Have a responsible informant Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR) criteria for Dementia of the Alzheimer's type
  • •6. National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) criteria for probable Alzheimer's disease (AD)
  • •7. Mini-Mental State Examination (MMSE) between 15 and 24

排除标准

  • •1. Inpatients
  • •2. Female patients of child-bearing potential
  • •3. Dementia due to any condition other than AD
  • •4. History of epilepsy or solitary seizure
  • •5. History or presence of Parkinson's disease or Parkinsonism
  • •6. Major neurological or neurodegenerative conditions associated with significant cognitive impairment such as Multiple Sclerosis or Huntington's Disease
  • •7. Major psychiatric conditions

研究者

发起方
Institut de Recherches Internationales Servier (France)

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