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Clinical Trials/CTRI/2020/06/026055
CTRI/2020/06/026055
Not yet recruiting
Phase 3

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 sites0 target enrollmentTBD
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Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Ministry of AYUSH
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •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.

Exclusion Criteria

  • •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.

Outcomes

Primary Outcomes

Not specified

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