Created at Source Raw Value Validated value
Nov. 16, 2021, 6:30 p.m. usa

inclusion criteria for enrollment: patients ≥18 years of age hospitalized with covid-19 enrolled within 72 hours of hospitalization or within day 14 from first signs of illness pulmonary infiltrates on chest imaging oxygenation of <95% on room air laboratory confirmed covid-19 exclusion criteria contraindication to transfusion due to inability to tolerate additional fluid, such as due to decompensated congestive heart failure baseline requirement for oxygen supplementation prior to covid-19 infection or use of positive pressure therapy for sleep disordered breathing currently experiencing severe hypoxemic failure, as defined in study endpoints prior receipt of plasma products, ivig, or hyperimmune globulin within past 3 months not currently enrolled another interventional clinical trial of covid-19 treatment. note: if taking medications with potential anti-covid activity for the purpose of covid-19 treatment that do not yet have data to support efficacy, such as il-6 antagonists, these medications must be stopped prior to enrollment. receipt of current standard of care covid-19 treatment, including remdesivir and dexamethasone is permitted and should be recorded as a concomitant medication. note: pregnancy is not exclusionary but will merit additional discussion of risks & benefits in the context of ongoing pregnancy

inclusion criteria for enrollment: patients ≥18 years of age hospitalized with covid-19 enrolled within 72 hours of hospitalization or within day 14 from first signs of illness pulmonary infiltrates on chest imaging oxygenation of <95% on room air laboratory confirmed covid-19 exclusion criteria contraindication to transfusion due to inability to tolerate additional fluid, such as due to decompensated congestive heart failure baseline requirement for oxygen supplementation prior to covid-19 infection or use of positive pressure therapy for sleep disordered breathing currently experiencing severe hypoxemic failure, as defined in study endpoints prior receipt of plasma products, ivig, or hyperimmune globulin within past 3 months not currently enrolled another interventional clinical trial of covid-19 treatment. note: if taking medications with potential anti-covid activity for the purpose of covid-19 treatment that do not yet have data to support efficacy, such as il-6 antagonists, these medications must be stopped prior to enrollment. receipt of current standard of care covid-19 treatment, including remdesivir and dexamethasone is permitted and should be recorded as a concomitant medication. note: pregnancy is not exclusionary but will merit additional discussion of risks & benefits in the context of ongoing pregnancy

Oct. 26, 2020, 11:31 p.m. usa

inclusion criteria for enrollment: 1. patients ≥18 years of age 2. hospitalized with covid-19 3. enrolled within 72 hours of hospitalization or within day 14 from first signs of illness 4. pulmonary infiltrates on chest imaging 5. oxygenation of <95% on room air 6. laboratory confirmed covid-19 exclusion criteria 1. contraindication to transfusion due to inability to tolerate additional fluid, such as due to decompensated congestive heart failure 2. baseline requirement for oxygen supplementation prior to covid-19 infection or use of positive pressure therapy for sleep disordered breathing 3. currently experiencing severe hypoxemic failure, as defined in study endpoints 4. prior receipt of plasma products, ivig, or hyperimmune globulin within past 3 months 5. not currently enrolled another interventional clinical trial of covid-19 treatment. note: if taking medications with potential anti-covid activity for the purpose of covid-19 treatment that do not yet have data to support efficacy, such as il-6 antagonists, these medications must be stopped prior to enrollment. receipt of current standard of care covid-19 treatment, including remdesivir and dexamethasone is permitted and should be recorded as a concomitant medication. note: pregnancy is not exclusionary but will merit additional discussion of risks & benefits in the context of ongoing pregnancy

inclusion criteria for enrollment: 1. patients ≥18 years of age 2. hospitalized with covid-19 3. enrolled within 72 hours of hospitalization or within day 14 from first signs of illness 4. pulmonary infiltrates on chest imaging 5. oxygenation of <95% on room air 6. laboratory confirmed covid-19 exclusion criteria 1. contraindication to transfusion due to inability to tolerate additional fluid, such as due to decompensated congestive heart failure 2. baseline requirement for oxygen supplementation prior to covid-19 infection or use of positive pressure therapy for sleep disordered breathing 3. currently experiencing severe hypoxemic failure, as defined in study endpoints 4. prior receipt of plasma products, ivig, or hyperimmune globulin within past 3 months 5. not currently enrolled another interventional clinical trial of covid-19 treatment. note: if taking medications with potential anti-covid activity for the purpose of covid-19 treatment that do not yet have data to support efficacy, such as il-6 antagonists, these medications must be stopped prior to enrollment. receipt of current standard of care covid-19 treatment, including remdesivir and dexamethasone is permitted and should be recorded as a concomitant medication. note: pregnancy is not exclusionary but will merit additional discussion of risks & benefits in the context of ongoing pregnancy