CTRI/2021/05/033623尚未招募4 期
Documentation of efficacy of select AYUSH Interventions Ayush-64 and Kabasura Kudineer in asymptomatic & mild to moderate Covid-19 patients in home isolation. - NA
Ministry of AYUSH Govt of India0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
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
- •Individuals of any gender within the age group 18-60 years
- •Individuals diagnosed as COVID 19 and categorized as asymptomatic, mild or moderate disease
- •within < One week of confirmation of COVID 19 disease
- •Patients in home isolation under standard care as per the government guidelines
- •Patients providing informed consent and willing to participate in the clinical study
排除标准
- •Patients not willing to use the Ayush interventions(AYUSH-64 &KabasuraKudineer)
- •Pregnant, lactating women and other vulnerable population
- •Use of immunosuppressive doses of corticosteroids prior to the enrollment in the study and planned use of immunosuppressive doses of corticoids
- •Any other condition that, in the opinion of the principal investigator or his/her representative physician, could put the safety of potential participants at risk or prevent them from complying with this protocol.
- •Patients who were diagnosed as having severe disease or receiving oxygen support.
- •People who are unable to take oral medication
- •People whose SpO2 levels are fluctuating within the range of 90-94.
研究者
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