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Clinical Trial Summary

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) promotes challenging immune and inflammatory phenomena. Though various therapeutic possibilities have been tested against coronavirus disease 2019 (COVID-19), the most adequate treatment has not yet been established. Among candidate adjunct treatment options, propolis, produced by honey bees from bioactive plant exudates, has shown potential against viral targets and has demonstrated immunoregulatory properties.


Clinical Trial Description

To evaluate the efficacy and safety of oral propolis as an adjunct treatment for SARS-CoV-2 infection, we designed a randomized, double-blind, placebo-controlled trial (Bee-Covid2) (The Use of Brazilian Green Propolis Extract (EPP-AF®) in Patients Affected by COVID-19). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04800224
Study type Interventional
Source D'Or Institute for Research and Education
Contact
Status Completed
Phase Phase 2/Phase 3
Start date April 12, 2021
Completion date July 30, 2021

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