<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(1)</volume><submitter>Manzini PM</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The efficacy of early treatment with convalescent plasma in patients with COVID-19 is debated. Nothing is known about the potential effect of other plasma components other than anti-SARS-CoV-2 antibodies.&lt;h4>Methods&lt;/h4>To determine whether convalescent or standard plasma would improve outcomes for adults in early phase of Covid19 respiratory impairment we designed this randomized, three-arms, clinical trial (PLACO COVID) blinded on interventional arms that was conducted from June 2020 to August 2021. It was a multicentric trial at 19 Italian hospitals. We enrolled 180 hospitalized adult patients with COVID-19 pneumonia within 5 days from the onset of respiratory distress. Patients were randomly assigned in a 1:1:1 ratio to standard of care (n = 60) or standard of care +</pubmed_abstract><journal>BMC infectious diseases</journal><pagination>879</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9682750</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Convalescent or standard plasma versus standard of care in the treatment of COVID-19 patients with respiratory impairment: short and long-term effects. 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A three-arm randomized controlled clinical trial.</name><description>&lt;h4>Background&lt;/h4>The efficacy of early treatment with convalescent plasma in patients with COVID-19 is debated. Nothing is known about the potential effect of other plasma components other than anti-SARS-CoV-2 antibodies.&lt;h4>Methods&lt;/h4>To determine whether convalescent or standard plasma would improve outcomes for adults in early phase of Covid19 respiratory impairment we designed this randomized, three-arms, clinical trial (PLACO COVID) blinded on interventional arms that was conducted from June 2020 to August 2021. It was a multicentric trial at 19 Italian hospitals. We enrolled 180 hospitalized adult patients with COVID-19 pneumonia within 5 days from the onset of respiratory distress. Patients were randomly assigned in a 1:1:1 ratio to standard of care (n = 60) or standard of care +</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-05-28T20:54:24.594Z</modification><creation>2024-12-03T16:22:03.824Z</creation></dates><accession>S-EPMC9682750</accession><cross_references><pubmed>36418984</pubmed><doi>10.1186/s12879-022-07716-5</doi></cross_references></HashMap>