跳至主要内容
临床试验/KCT0007062
KCT0007062尚未招募未知

Evaluation of clinical effectiveness of choline alphoscerate for older adults with major depression and subjective memory complaints: a double-blinded, placebo-controlled, Randomization, multicenter Investigator-initiated trial

Samsung Medical Center0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
60(Year) 至 o Limit(—)
性别
All

入选标准

  • 1) Age = 60 years
  • 2) Diagnosed as MDD under the criteria of Diagnostic and Statistical Manual of Mental Disorders (DSM-5) and confirmed with MINI-Depression
  • 3) HAM-D = 14
  • 4) MMSE = 20
  • 5) Who had continuous subjective memory complaints more than 6 months before the period of screening
  • 6) Who had taking antidepressants longer than 1 month in the period of screening

排除标准

  • 1) Diagnosed as schizophrenia, bipolar disorder, PTSD, OCD or other significant mental disorder under the criteria of DSM-5 (only the participants who had depressive disorder, sleep disorder, and the anxiety disorder are allowed to be included)
  • 2) Who have medically unstable disease (only the participants, who have diabetes mellitus or hypertension under control with stable medication for 3 months could be included)
  • 3) Diagnosed as dementia or mild cognitive impairment
  • 4) Participants who are already taking choline alfoscerate within 6 months of period
  • 5) Participants who have been taking medication of antipsychotics (including quetiapine), mood stabilizer, cognitive enhancer including donepezil, rivastigamine, galantamine, and memantine within 1months.
  • 6) Participants who had previous history of liver disease or renal disease
  • 7) Participants who had allergic reaction to choline alfoscerate
  • 8) Other specific condition, which could be inappropriate for the trial inclusion, under the judgement of the principal investigator

研究者

相似试验