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
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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