None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Subject willing to give voluntary informed consent 2. Irrespective Sex 3. Healthy Volunteers 4. Health Workers 5. Front line workers during pandemic 6. Subject having travelling history 7. Subject willing to follow the procedure as per the study protocol
Exclusion criteria
Exclusion criteria: 1. COVID 19 positive patient 2. Fever 3. Hypersensitivity or idiosyncratic reaction to any drugs or herbal products 4. History of allergic condition 5. History of psychiatric disorder 6. Presence of abnormal laboratory report 7. Known subject of malignancy 8. Subject of participating in another clinical study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1-Number of individuals developing symptoms 2-Number of individuals turning COVID 19 test positiveTimepoint: 0-enrollment of patient for intervention(baseline) Follow up after 2 weeks. Outcome will be assessed 1-Baseline- 2nd-after 4 week 3rd - after 6 week 4th-after 8 week 5th -after 10 week 6th- after 12 week | — |
Secondary
| Measure | Time frame |
|---|---|
| 1 Number of individuals developing symptoms. 2 Number of individuals turning COVID 19 test positive. 3 Adverse events. 4 Improvement in immune status using immune status qustionnaire.Timepoint: secondary outcome will be assessed after 6 month from baseline. | — |
Countries
India
Contacts
Shree Saptashrungi Ayurved Mahavidyalaya and Hospital