Name (Synonyms) | Correlation |
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There is one clinical trial.
We hypothesize that early institution of TNFα inhibitor therapy in patients with severe COVID-19 infections will prevent further clinical deterioration and reduce the need for advanced cardiorespiratory support and early mortality. To address this hypothesis, a prospective, single center, phase 2 trial is proposed to assess the efficacy of infliximab or infliximab-abda in hospitalized adult patients with severe or critical COVID-19. Observations from this study will inform the conduct of prospective randomized controlled studies to follow.
Description: Time to improvement in oxygenation
Measure: Time to improvement in oxygenation Time: 28 DaysDescription: 28-day mortality
Measure: 28-day mortality Time: 28 DaysDescription: Assessment of cytokine and inflammatory profile at baseline and at 48 hours after therapy
Measure: Assessment of cytokine and inflammatory profile at baseline and at 48 hours after therapy Time: 28 DaysDescription: Qualitative and quantitative toxicity
Measure: Qualitative and quantitative toxicity Time: 28 DaysDescription: incidence and duration of supplemental oxygen administration by nasal cannula, simple face mask, or other similar oxygen delivery device
Measure: incidence and duration of supplemental oxygen administration Time: 28 DaysDescription: Incidence and duration of non-invasive ventilation or by non-rebreather mask or high-flow nasal cannula
Measure: Incidence and duration of non-invasive ventilation or by non-rebreather mask or high-flow nasal cannula Time: 28 DaysDescription: Incidence and duration of mechanical ventilation
Measure: Incidence and duration of mechanical ventilation Time: 28 DaysDescription: Incidence and duration of vasopressor support
Measure: Incidence and duration of vasopressor support Time: 28 DaysDescription: Incidence and duration of extracorporeal membrane oxygenation
Measure: Incidence and duration of extracorporeal membrane oxygenation Time: 28 DaysDescription: Duration of fever
Measure: Duration of fever Time: 28 DaysDescription: Correlation of cytokine profile to clinical outcomes specified in primary and secondary objectives
Measure: Correlation of cytokine profile to clinical outcomes specified in primary and secondary objectives Time: 28 DaysDescription: Duration of hospitalization
Measure: Duration of hospitalization Time: 28 DaysDescription: Secondary infections
Measure: Secondary infections Time: 28 Days