Coronavirus Infections
Conditions
Interventions
The total of 240 participants, 120 in each group, placebo and agent.The number of shots (twice daily) and the duration of treatment (14 days) follow the regimen in clinical studies that evaluated the
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Sponsors
Universidade Federal do Rio Grande do Sul
Universidade Federal do Rio Grande do Sul
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Older than 18 years; suspected coronavirus infection
Exclusion criteria
Exclusion criteria: Hospital internment; intolerance to the tested compounds; unwillingness to use teas daily; pregnant women or women of reproductive age who do not use hormonal contraceptives.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in the number of days of symptoms such as cough, dyspnea and headache, assessed by questionnaire and daily follow-up. Data collected on the first day of tea drinking and throughout the 14 days daily. | — |
Secondary
| Measure | Time frame |
|---|---|
| 50% reduction in cough days, measured through daily questionnaires over the 14 days of intervention | — |
Countries
Brazil
Contacts
Public ContactCaroline Dani
Outcome results
None listed