Last updated: May 11, 2022
Sponsor: D'Or Institute for Research and Education
Overall Status: Completed
Phase
2/3
Condition
Inflammation
Covid-19
Treatment
N/AClinical Study ID
NCT04800224
31099320.6.0000.0049
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Older than 18 years;
- Diagnosis of coronavirus infection confirmed by polymerase chain reaction - reversetranscriptase testing;
- Symptoms started within 14 days of the randomization date
Exclusion
Exclusion Criteria:
- Pregnant or lactating women;
- Known hypersensitivity to propolis;
- Propolis use less than 30 days from the randomization date;
- Active cancer;
- Human immunodeficiency virus carriers;
- Patients undergoing transplantation of solid organs or bone marrow or who were usingimmunosuppressive medications;
- Bacterial infection at randomization, sepsis or septic shock related to bacterialinfection at randomization;
- Impossibility of using the medication orally or by nasoenteral tube;
- Known hepatic failure or advanced heart failure (New York Heart Association [NYHA]class III or IV).
- End Stage Renal Disease (ESRD).
Study Design
Total Participants: 200
Study Start date:
April 12, 2021
Estimated Completion Date:
July 30, 2021
Study Description
Connect with a study center
Hospital Sao Rafael
Salvador, BA 41820340
BrazilSite Not Available
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