To determinate feasibility, safety and outcome with convalescent plasma in patients with severe COVID-19 penumonia
COVID-19 convalescent plasma will be infused to patients with severe COVID-19 pneumonia to determine feasibility, safety and clinical outcome efficacy by survival at-28 days. Data will be compared with match control arm patients without plasma infusion
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
200
intravenous infusion of 300-600 mL of convalescent plasma with an antibody title more than 3 according to chemiluminescent microparticle immunoassay (Architect Plus Abbott)
Centro de Educación Médica e Investigaciones Clínicas
Buenos Aires, Argentina
28 days survival
number of subjects surviving at 28 days from plasma infusion
Time frame: 28 days
efficacy of plasma infusion according to antibodies levels in the infuse bags
comparison of clinical efficacy according antibodies levels
Time frame: 28 days
clinical efficacy of plasma infusion according to frame time from symptoms onset and hospitalization
we will search if clinical efficacy is better when the earlier the infusion is decided
Time frame: 28 days
change in clinical WHO ordinal scale from 1 to 10 points
WHO clinical scale is a measure of patient progression through the health-care system with 1 point asymptomatic patient and 10 patient dead
Time frame: 14 days
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