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Clinical Trials/CTRI/2022/02/040156
CTRI/2022/02/040156
Not yet recruiting
Phase 3

A prophylactic community based study to assess the impact of Ayuraksha Kit in COVID-19

Central council for research in Ayurvedic Sciences0 sites0 target enrollmentTBD
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Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Central council for research in Ayurvedic Sciences
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

  • •i.Participants not having COVID\-19 like symptoms, of age between 18 â?? 70 years, of any sex from the identified scheduled castes predominant areas/villages across India
  • •ii.Participants who are ready to provide informed consent.
  • •iii.Participants who have been either vaccinated or not vaccinated shall be included in the study.
  • •iv.Participants who have been taking any other prophylactic medicine other than Ayu Raksha kit for COVID \-19 shall also be included. The details will be noted and data will be analysed accordingly

Exclusion Criteria

  • •i.Participants presenting with COVID\-19 like symptoms
  • •ii.Participants diagnosed as case of COVID\-19 by positive RT\-PCR test within one month prior to inclusion.
  • •iii.History of uncontrolled Diabetes mellitus or uncontrolled Hypertension
  • •iv.Participants having any disease condition that would require immediate medical or surgical intervention
  • •v.Known case of immune compromised state like HIV
  • •vi.Known cases of COPD, Tuberculosis, Cancer, Hepatitis
  • •vii.Participants on steroids or any immunosuppressive therapy
  • •viii.Those who have participated in any other clinical trial within one month prior to screening
  • •ix.Participants having a history of allergy to any medicine that is part of Ayu Raksha Kit
  • •x.Women who are Pregnant or are planning for pregnancy during the study period or those who are lactating mothers

Outcomes

Primary Outcomes

Not specified

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