CTRI/2019/03/018074已完成未知
Clinical Evaluation of Ashwagandha Standardized Extract (KSM 66) for itsPharmacological Actions on Sleep in Subjects Having Insomnia and HealthySubjects: A Prospective, Randomized, Double-Blind, Placebo-Controlled Study
Dr D Y Patil Medical College Hospital and Research Center0 个研究点目标入组 80 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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. Diagnosis of insomnia based on DSM-IV criteria
- •2. More than 30 minutes to fall asleep and subjective total sleep time of ââ?°Â¤6.5 hours per night (for at least 3 nights per week); and daytime complaints associated with disturbed sleep
- •3. Habitual bedtime between 8.30 pm to midnight
- •4. Body Mass Index between 16.5 to 30 kg/sq.m.
- •5. Subjects able to understand the sleep diary and are able to and willing to fill the sleep log diary and follow other procedures required by the study protocol
- •6. Subjects who sign the informed written consent
排除标准
- •1. Pregnant or breast-feeding women or women with positive urinary pregnancy test at screening.
- •2. Known clinically significant endocrine, metabolic, hepatic, renal, cardiovascular, gastrointestinal, respiratory, haematological or neurological illnesses.
- •3. Presence of any current psychiatric disorders that are judged by investigator as potentially causing or contributing to insomnia.
- •4. Subjects who suffer from sleep disorder other than primary insomnia including restless leg syndrome and sleep apnea.
- •5. Substance dependence/ abuse in the past one year or with alcohol abuse are ineligible.
- •6. Those using tobacco products during night awakenings.
- •7. History of seizures or significant head trauma.
- •8. Subjects who travelled across four or more time zones or worked on night or rotating shifts in previous 7 days before study initiation or who plan to do the same during the study period.
- •9. Currently taking any medication on a regular basis (except for antihypertensives, antidiabetics, lipid lowering agents and drugs for primary cardiovascular prophylaxis).
- •10. Any other investigational drug was used within three months prior the entry in this study.
- •11. Those who cannot be relied upon to comply with the test procedures or are unwilling to give informed consent.
研究者
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