Name (Synonyms) | Correlation |
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Name (Synonyms) | Correlation |
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There is one clinical trial.
This is a single arm, open label study designed to evaluate the safety and efficacy of etoposide in patients with the 2019 novel coronavirus (COVID-19) infection. Treatment will be comprised of etoposide administered intravenously at a dose of 150 mg/m2 on Days 1 and 4 as prevention of cytokine storm in patients with COVID-19 infection.
Description: An 8 point ordinal scale will be used to assess pulmonary status consisting of the following values: 8= Death; 7= Ventilation in addition to extracorporeal membrane oxygen (ECMO), continuous renal replacement therapy (CRRT), or need for vasopressors (dopamine ≥5 μg/kg/min OR epinephrine ≥0.1 μg/kg/min OR norepinephrine ≥0.1 μg/kg/min); 6= Intubation and mechanical ventilation; 5= Non-invasive mechanical ventilation (NIV) or high-flow oxygen; 4= Oxygen by mask or nasal prongs; 3= Hospitalization without oxygen supplementation; 2= Discharged from hospital either to home with supplemental oxygen OR to inpatient rehabilitation/skilled nursing facility (+/- supplemental oxygen); 1= Discharged to home without supplemental oxygen
Measure: Change in pulmonary status Time: baseline, through study completion, an average of 45 daysDescription: number of events
Measure: Incidence of serious adverse events Time: baseline, through study completion, an average of 45 daysDescription: When calculating days of hospitalization, re-hospitalization or death occurring in the first 28 days should result in zero ascribed to time out of the hospital prior to readmission.
Measure: Length of hospitalization Time: From date of enrollment until the date of extubation, assessed study completion, an average of 45 daysDescription: Reintubations or death within 28 days will result in zero ascribed time off ventilator prior to reintubation
Measure: Ventilator free days Time: baseline, through study completion, an average of 45 days