CTRI/2021/06/034132已完成2 期
A Double blind, randomized, placebo controlled clinical trial to evaluate safety and efficacy of ShatPlus as an intervention in subjects with SARS-CoV-2 Infection. - Nil
BVG Life Sciences Ltd BVG Group0 个研究点目标入组 60 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 60
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.Age :18- 60 years (Both sex)
- •2.Confirmed COVID 19 Subject with positive RT-PCR
- •3.Mild to moderate disease (NEWS score <7) with or without comorbidity
- •4.Subject willing to provide consent and follow up for study duration
排除标准
- •1.Subjects with compromised immunity, autoimmune disease or self-reports HIV or syphilis infection
- •2.Proves to be unfit for the study as per the investigatorâ??s discretion
- •3.Pregnant or lactating women
- •4.Requiring supplemental oxygen and ICU admission at screening
- •5.Known case of comorbidity which is uncontrolled and which in investigator discretion finds subject not suitable for the trial participation
- •6.Any other medical condition like History of MI, Epileptic episodes finding subject not fit for trial participation
研究者
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