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Clinical Trial Summary

Aim of the study is to verify the efficacy and safety of convalescent hyperimmune plasma infusion in hospitalized covid-19 patients non in ITU with pneumonia and respiratory symptoms within seven days from the beginning of symptoms. Efficacy is evaluated by the number of patients who will improve their clinical condition and will not be admitted to ITU. .Safety is considered in relation to adverse reactions to plasma infusion.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04622826
Study type Interventional
Source Azienda USL Toscana Nord Ovest
Contact mirko lombardi
Phone 00393478546332
Email mirkolombardi9@gmail.com
Status Recruiting
Phase Phase 2
Start date May 15, 2020
Completion date December 31, 2020

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