CTRI/2021/02/031256已完成2 期
Clinical validation of safety & efficacy of Madhav Rasayan Plus in subjects of COVID 19. - Nil
Shree Vishwavati Ayurvedic Chikitsalaya and Research Centre0 个研究点目标入组 40 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
- 40
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
- •Age -18- 60 years (Both sex)
- •Confirmed COVID 19 patient with positive RT-PCR
- •Moderate to severe symptomatic patients having no signs of ARDS (NEWS score <=8)
- •Subject willing to provide consent and follow up for study duration
排除标准
- •Patients with autoimmune disease or self-reports HIV or syphilis infection
- •Proves to be unfit for the study as per the investigatorâ??s discretion
- •Pregnant or lactating women
- •Requiring ICU admission at screening
- •Any other comorbidity which is critical stage at screening which in investigator discretion finds subject not suitable for the trial participation
研究者
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