CTRI/2020/06/025855已完成2 期
Efficacy of Ayurveda Intervention (AYUSH 64) as add-on therapy in COVID 19 patients - An open label randomized controlled trial
IPGT and RA0 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
- 2 期
- 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
- •Asymptomatic or minimal symptomatic COVID 19 patients Patients having 0 to 4 score as per the WHO ordinal scale for clinical improvement
- •Age 18 to 70years
- •Patients who can take oral medicine
- •Patients who are ready to give written consent
排除标准
- •Age below 18 and above 70years
- •Patients having severe symptoms of COVID19
- •Patients on mechanical ventilator or organ support
- •Patients do not able to take oral medication
- •Pregnant and lactating women
- •Oncological diseases and other systemic uncontrol conditions such as HTN diabetes etc
- •Liver or kidney malfunctions.
- •Severe pneumonia Acute respiratory distress syndrome Sepsis and Septic Shock
研究者
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