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临床试验/CTRI/2016/10/007354
CTRI/2016/10/007354已完成4 期

Efficacy And Safety Of KSM66 Ashwagandha (Withania somnifera) In Cognitive Function In Healthy Adults: A prospective, Randomized, Double blind, Placebo controlled Study

Shri Kartikeya Pharma0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
入组人数
50

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

入选标准

  • 1.Adult male or female patients aged greater than 35 years of age
  • 2.Patients with early dementia or mild cognitive impairment
  • 3.Have a screening Mini-Mental State Examination (MMSE) score of greater than or equal to 19 (mild or no memory impairment)
  • 4.Patients with subjective memory complaints
  • 5.Have the ability to understand the requirements of the study
  • 6.Participants agree to abide by the study restrictions and return for the required assessments
  • 7.Participants willing to sign informed consent

排除标准

  • 1 Have a screening Mini-Mental State Examination (MMSE) score of less than 19(moderate and severe memory impairment)
  • 2.Psychiatric with known neuropsychiatric conditions like Schizophrenia, Parkinsonism, Huntingtonâ??s disease, Picks disease etc.
  • 3.Patients taking psychotropic drugs including alcohol
  • 4.Patients taking any other drugs or alternative medicines for enhancement of memory
  • 5.Patients with known persistent endocrine disorders
  • 6.Patients with uncontrolled hypertension
  • 7.Patients with uncontrolled diabetes mellitus
  • 8.H/o of drug dependence or any severe co-morbid medical conditions
  • 9.Pregnant and lactating women
  • 10.Subjects with known hypersensitivity to Ashwagandha
  • 11.History of major surgery within the past 6 months
  • 12.Participation in other clinical trials during previous 3 months
  • 13.Any clinical condition, according to the investigator which does not allow safe fulfillment of the study protocol

研究者

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