Developed by Shray Alag, The Harker School
Sections: Correlations,
Clinical Trials, and HPO
Navigate: Clinical Trials and HPO
Navigate: Correlations HPO
There is one clinical trial.
The COVID-19 pandemic is of grave concern due its impact on human health and on the economy. Propolis, a natural resin produced by bees from plant materials, has anti-inflammatory, immunomodulatory, anti-oxidant properties, and various aspects of the SARS-CoV-2 infection mechanism are potential targets for propolis compounds. Propolis components have inhibitory effects on the ACE2, TMPRSS2 and PAK1 signaling pathways; in addition, antiviral activity has been proven in vitro and in vivo. This is a pilot randomized study that aims to assess the impact of using Brazilian green propolis extract against the deleterious effects of the new coronavirus.
Description: Composite clinical outcome with oxygen therapy dependency time (in days) or hospitalization time (in days) after randomization.
Measure: Composite clinical outcome with oxygen therapy dependency time or hospitalization time Time: 1-28 daysDescription: We will evaluate the presence or absence of symptoms related to the use of propolis through a questionnaire.
Measure: Percentage of participants with adverse events during the use of propolis Time: 1-28 daysDescription: Assess the degree of acute kidney injury according to KDIGO (through serum creatinine or urine output).
Measure: Rate and severity of acute kidney injury during the study Time: 1-28 daysDescription: Assess need or not for renal replacement therapy.
Measure: Renal replacement therapy. Time: 1-28 daysDescription: Describe the time needed for vasopressors in days after randomization
Measure: Rate of need for vasopressor use Time: 1-28 daysDescription: Assess length of stay in the ICU after randomization in days
Measure: Need for intensive care unit (ICU) Time: 1-28 daysDescription: Rate of readmission to the ICU after randomization
Measure: Intensive care unit (ICU) readmission Time: 1-28 daysDescription: Assess the need for mechanical ventilation in days after randomization.
Measure: Invasive oxygenation time Time: 1-28 daysDescription: Evaluate the variation in serum levels of c-reactive protein over the 7 days after randomization
Measure: Variation of plasma c-reactive protein Time: 1-7 daysAlphabetical listing of all HPO terms. Navigate: Correlations Clinical Trials
Data processed on September 26, 2020.
An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.
Drug Reports MeSH Reports HPO Reports