CTRI/2018/01/011170已完成未知
â??A Prospective, Interventional, Single center, Randomised, Double blind, Placebo Controlled, clinical study to evaluate the Efficacy & Safety of Instavit® instant energy oral spray in the implications on health and performance on everyday fatigue condition and improvement of alertnessâ??.
Instavit Ltd0 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
- 未知
- 状态
- 已完成
- 发起方
- 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. Mentally, physically and legally eligible to give informed consent.
- •2. Male and female BMI between 20.0 â?? 25.9 kg/m2
- •3. Subject meet criteria for fatigue as per Chalder Fatigue Assessment scale.
- •4. Subjects willing and able to provide informed consent voluntarily
- •5. Patient is willing and able to comply with all trial requirements
排除标准
- •1. Significant medical or psychiatric illness
- •2. Subjects having history of drug or alcohol abuse
- •3. Previous receipt of Study Drug
- •4. History of HIV, HAV, HBs Ag
- •5. Volunteers who have participated in any drug research study within past 3 months.
- •6. Presence or history of hypersensitivity to any of the active or inactive ingredients
- •7. Pregnant or lactating women
研究者
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