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Clinical Trial Summary

To determinate feasibility, safety and outcome with convalescent plasma in patients with severe COVID-19 penumonia


Clinical Trial Description

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 Design


Related Conditions & MeSH terms


NCT number NCT04535063
Study type Interventional
Source Centro de Educación Medica e Investigaciones Clínicas Norberto Quirno
Contact
Status Completed
Phase Phase 3
Start date April 18, 2020
Completion date February 25, 2021

See also
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