Ayurvedic Interventions in prevention of COVID-19 infection-A survey study
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1 Aged 18 to 70 years of both male or female
2 Residents of the identified containment zones, marked by Govt. of
NCT Delhi for high risk of COVID 19
3 Willing to take study medication;
4 Provides written informed consent prior to initiation of study
procedures (or legally authorized representative). Only the copy of
photography of informed consent would be kept for records.
1 Persons already treated with any of the study drugs during the last 30 days;
2 Pregnant and lactating females and those who have a pregnancy plan
3 Participants with any immunosuppressive medication or in an immune
compromised state or haematological disease.
4 Laboratory confirmed COVID-19 with or without symptoms.
5 Known allergy to any of the medications used in this trial.
6 Not willing to participate in the study.
7 Any other criteria, as per the investigator would jeopardize the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of COVID 19 positive cases (as confirmed by hospital by standard investigation (real-time polymerase chain reaction test) among Ayurveda usersTimepoint: 3)After enrolment on day one, assessment will be done on day 7, 15, 22 and 30 by telephonic communication or as convenient to the participant.
- Secondary Outcome Measures
Name Time Method 1)Incidence of severe COVID 19 positive cases among Ayurveda users <br/ ><br>2)Incidence of mortality due to COVID 19 among Ayurveda users. <br/ ><br>3)Incidence of any other ailment like cough, fever, sore throat etc during this study <br/ ><br>4)Change in appetite, bowel habit, sleep among the users. <br/ ><br>5)ADR/AE due to use of any particular Ayurveda advocaciesTimepoint: After enrolment on day one, assessment will be done on day 7, 15, 22 and 30 by telephonic communication or as convenient to the participant.