None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) All healthcare professionals and staff of age group between 25 to 60 years willing to participate, negative for SARS- Cov-2 at screening,(tested by rt-PCR) without co-morbid condition
Exclusion criteria
Exclusion criteria: 1) Pregnant and lactating females. 2) Immune compromised and co morbid condition cases. 3)Laboratory confirmed COVID-19 with or without symptoms 4)Known allergy to any of the medications used in this trial. 5) Subjects who are taking any other medicine as prophylaxis such as HCQ.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of participants with SARS- Cov-2 positivity as estimated by RT-PCR of nasopharyngeal swabTimepoint: baseline Day 30 | — |
Secondary
| Measure | Time frame |
|---|---|
| Safety profile of the intervention as estimated by LFT, KFT and other haematological & biochemical investigations. Presence or absence of AE/ADR. Number of participants who developed any infective diseases during the trial period (bacterial /viral/ fungal / etc.) and percentage of participants with Upper respiratory tract illness during the period. Timepoint: baseline Day 7 Day 15 Day 30 | — |
Countries
India
Contacts
Chaudhary Bahm Prakash Ayurved Charak Sansthan