跳至主要内容
临床试验/EUCTR2009-011881-27-DE
EUCTR2009-011881-27-DE
进行中(未招募)
不适用

Changes of cerebral spinal fluid APPSa levels under oral therapy with acitretin 30 mg daily in patients with mild to moderate Alzheimer’s disease: a multicenter prospective randomised placebo-controlled parallel-group study. - Alzheimer´s Disease Acitretin Medication (ADAM)

niversity Medical Center of the Johannes Gutenberg-University Mainz0 个研究点2010年1月20日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Alzheimer’s disease
发起方
niversity Medical Center of the Johannes Gutenberg-University Mainz
状态
进行中(未招募)
最后更新
11年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2010年1月20日
结束日期
待定
最后更新
11年前
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

发起方
niversity Medical Center of the Johannes Gutenberg-University Mainz

入排标准

入选标准

  • mild to moderate AD (NINCDS\-ADRDA criteria)
  • MMSE according to Folstein: 27\-14 points
  • Geriatric Depression Scale \= 14
  • age \= 50 years
  • ability of subject to understand character and individual consequences of clinical trial
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 38
  • F.1\.3 Elderly (\>\=65 years) yes

排除标准

  • hereditary cognitive impairment
  • known history of brain injuries
  • Insufficient German language skills
  • actual treatment with other potential disease modifying drugs of AD
  • multimorbidity or significant organ (esp. liver or renal) dysfunction
  • evidence of Non\-AD neurodegenerative disorder (e.g. Parkinson)
  • contraindication to acitretin such as osteoporosis, hypoalbuminaemia

结局指标

主要结局

未指定

相似试验