跳至主要内容
临床试验/CTRI/2021/05/033623
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

发起方
Ministry of AYUSH Govt of India

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