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临床试验/CTRI/2020/06/026055
CTRI/2020/06/026055尚未招募3 期

A prospective interventional study on the effect of ASA-20(Ayush kwath, Samsamani vati, Anu taila) as a prophylaxis measure among High risk population exposed to COVID-19 - ASA-20

Ministry of AYUSH0 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
3 期
状态
尚未招募

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 Subjects of high risk population
  • 2 Male or female subjects above the age of 15 years to 70 years.
  • 3 Subjects who are ready to provide written/digital informed consent and who are willing to participate and follow the protocol requirements of the clinical study.

排除标准

  • 1 Pregnant and Lactating woman
  • 2 Subjects having any medical or surgical condition that would require immediate medical or surgical intervention at the time of screening.
  • 3 Subjects who are on any regular medication(alternative/modern) for any other ailments.
  • 4 Subjects participating in any other clinical study or having participated in any other study 1 month prior to screening in the present study.
  • 5 Subjects having a past history of allergy to any medicine that is part of the Ayurvedic intervention. Other conditions, which in the opinion of the investigators, makes the patient unsuitable for enrollment or could interfere with his participation in, and completion of the protocol.

研究者

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