None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthcare professionals and paramedic staff serving COVD-19 will be enrolled in the study. Inclusion criteria: a. All adult individuals of both sexes working in COVID-19 wards. b. Individuals willing to give informed consent c. Individuals with no prior history of COVID-19 infections d. Individuals currently not showing any symptoms of COVID-19 at the time of recruitment e. Individuals with no history and / or currently ongoing serious chronic health condition f. Willing to follow the protective majors as advised g. Willing to comply with the study protocol
Exclusion criteria
Exclusion criteria: a. Any history of allergy to turmeric and /or any of the ingredients used in making of the lozenge. b. Refusal for informed consent. c. Concurrent ongoing other infections. d. Any current medical history that investigator may consider not advisable to work in COVID-19 ward.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical acceptability of turmeric lozenges in COVID-19 healthcare teamsTimepoint: DAY 15 (follow up 1) and DAY 30 (end of study) are evaluation time points. | — |
Secondary
| Measure | Time frame |
|---|---|
| Safety and tolerance of turmeric lozengesTimepoint: End of study period at D 30 | — |
Countries
India
Contacts
Consultant, Gelnova Labs India Pvt Ltd.