<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>20(1)</volume><submitter>Cannata-Andia JB</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Vitamin D status has been implicated in COVID-19 disease. The objective of the COVID-VIT-D trial was to investigate if an oral bolus of cholecalciferol (100,000 IU) administered at hospital admission influences the outcomes of moderate-severe COVID-19 disease. In the same cohort, the association between baseline serum calcidiol levels with the same outcomes was also analysed.&lt;h4>Methods&lt;/h4>The COVID-VIT-D is a multicentre, international, randomised, open label, clinical trial conducted throughout 1 year. Patients older than 18 years with moderate-severe COVID-19 disease requiring hospitalisation were included. At admission, patients were randomised 1:1 to receive a single oral bolus of cholecalciferol (n=274) or nothing (n=269). Patients were followed from admission to </pubmed_abstract><journal>BMC medicine</journal><pagination>83</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8853840</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A single-oral bolus of 100,000 IU of cholecalciferol at hospital admission did not improve outcomes in the COVID-19 disease: the COVID-VIT-D-a randomised multicentre international clinical trial.</pubmed_title><pmcid>PMC8853840</pmcid><pubmed_authors>Fernandez-Martin JL</pubmed_authors><pubmed_authors>Herrero-Puente P</pubmed_authors><pubmed_authors>Palomo-Antequera C</pubmed_authors><pubmed_authors>Cunningham J</pubmed_authors><pubmed_authors>Panizo S</pubmed_authors><pubmed_authors>Naves-Diaz M</pubmed_authors><pubmed_authors>Mouzo R</pubmed_authors><pubmed_authors>Ibanez GH</pubmed_authors><pubmed_authors>Pefaur-Penna J</pubmed_authors><pubmed_authors>Douthat W</pubmed_authors><pubmed_authors>Cannata-Andia JB</pubmed_authors><pubmed_authors>Sanchez-Polo V</pubmed_authors><pubmed_authors>Gomez-Alonso C</pubmed_authors><pubmed_authors>Gomez MD</pubmed_authors><pubmed_authors>Cusumano CA</pubmed_authors><pubmed_authors>Carrillo-Lopez N</pubmed_authors><pubmed_authors>Ballarino C</pubmed_authors><pubmed_authors>Maderuelo-Riesco I</pubmed_authors><pubmed_authors>Calvino-Varela J</pubmed_authors><pubmed_authors>Fernandez P</pubmed_authors><pubmed_authors>COVID-VIT-D trial collaborators</pubmed_authors><pubmed_authors>Diaz-Sottolano A</pubmed_authors></additional><is_claimable>false</is_claimable><name>A single-oral bolus of 100,000 IU of cholecalciferol at hospital admission did not improve outcomes in the COVID-19 disease: the COVID-VIT-D-a randomised multicentre international clinical trial.</name><description>&lt;h4>Background&lt;/h4>Vitamin D status has been implicated in COVID-19 disease. The objective of the COVID-VIT-D trial was to investigate if an oral bolus of cholecalciferol (100,000 IU) administered at hospital admission influences the outcomes of moderate-severe COVID-19 disease. In the same cohort, the association between baseline serum calcidiol levels with the same outcomes was also analysed.&lt;h4>Methods&lt;/h4>The COVID-VIT-D is a multicentre, international, randomised, open label, clinical trial conducted throughout 1 year. Patients older than 18 years with moderate-severe COVID-19 disease requiring hospitalisation were included. At admission, patients were randomised 1:1 to receive a single oral bolus of cholecalciferol (n=274) or nothing (n=269). Patients were followed from admission to </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2026-05-31T01:19:27.324Z</modification><creation>2022-07-11T15:07:24.32Z</creation></dates><accession>S-EPMC8853840</accession><cross_references><pubmed>35177066</pubmed><doi>10.1186/s12916-022-02290-8</doi></cross_references></HashMap>