CTRI/2019/09/021415尚未招募2 期
An Open Label, Two Arm, Clinical Study to evaluate the Efficacy and Safety of HQAP061801 powder as an Oral Nutritional Supplement for Occupational Work Fatigue and Post Illness Convalescence
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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.Both male and female adult subjects between the age group of
- •2.More than 18 years to less than 60 years who are confirmed to have a history of work related fatigue as assessed through Fatigue assessment scale (FAS).
- •3.Both male and female adult subjects between the age group of More than 18 years to less than 60 years who are in post illness convalescence period.
- •4.Subject willing to refrain taking any other oral nutritional supplements during the study period.
- •5.Subjects willing to give written informed consent
- •Subjects who had not participated in similar kind of study in last 4 week.
排除标准
- •1.Subject with clinically significant systemic illnesses treated with medication.
- •2.Subject with chronic illness which need immediate therapeutic intervention.
- •3.Subjects with chronic infectious condition treated with medications
- •4.Subjects who are hypersensitive to any of the ingredients,
- •5.Pregnant & lactating women.
研究者
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