<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pessoa-Amorim G</submitter><funding>Health Data Research UK</funding><funding>Medical Research Council</funding><funding>NIHR Oxford Biomedical Research Centre</funding><funding>Foreign, Commonwealth and Development Office</funding><funding>National Institute for Health and Care Research</funding><funding>Bill and Melinda Gates Foundation</funding><funding>Oxford BHF Centre of Research Excellence</funding><funding>Medical Research Council Population Health Research Unit</funding><funding>Wellcome Trust</funding><funding>UK Research and Innovation</funding><funding>MRC Network of Hubs for Trials Methodology Research</funding><funding>National Center for Emerging and Zoonotic Infectious Diseases</funding><pagination>429</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11218071</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Randomised trials are essential to reliably assess medical interventions. Nevertheless, interpretation of such studies, particularly when considering absolute effects, is enhanced by understanding how the trial population may differ from the populations it aims to represent.&lt;h4>Methods&lt;/h4>We compared baseline characteristics and mortality of RECOVERY participants recruited in England (n = 38,510) with a reference population hospitalised with COVID-19 in England (n = 346,271) from March 2020 to November 2021. We used linked hospitalisation and mortality data for both cohorts to extract demographics, comorbidity/frailty scores, and crude and age- and sex-adjusted 28-day all-cause mortality.&lt;h4>Results&lt;/h4>Demographics of RECOVERY participants were broadly similar to the r</pubmed_abstract><journal>Trials</journal><pubmed_title>Clinical trial results in context: comparison of baseline characteristics and outcomes of 38,510 RECOVERY trial participants versus a reference population of 346,271 people hospitalised with COVID-19 in England.</pubmed_title><pmcid>PMC11218071</pmcid><funding_grant_id>RE/18/3/34214</funding_grant_id><funding_grant_id>MC_PC_19056</funding_grant_id><funding_grant_id>HDR-23012</funding_grant_id><funding_grant_id>MR/L004933/2</funding_grant_id><funding_grant_id>222406/Z/20/Z</funding_grant_id><pubmed_authors>Goldacre R</pubmed_authors><pubmed_authors>Stevens W</pubmed_authors><pubmed_authors>Mafham M</pubmed_authors><pubmed_authors>Haynes R</pubmed_authors><pubmed_authors>Morris EJA</pubmed_authors><pubmed_authors>Wallendszus K</pubmed_authors><pubmed_authors>Nunn M</pubmed_authors><pubmed_authors>Campbell M</pubmed_authors><pubmed_authors>Horby P</pubmed_authors><pubmed_authors>King A</pubmed_authors><pubmed_authors>Rees A</pubmed_authors><pubmed_authors>Crichton C</pubmed_authors><pubmed_authors>Murray D</pubmed_authors><pubmed_authors>Pinches H</pubmed_authors><pubmed_authors>Harper C</pubmed_authors><pubmed_authors>Pessoa-Amorim G</pubmed_authors><pubmed_authors>Peto L</pubmed_authors><pubmed_authors>Welsh R</pubmed_authors><pubmed_authors>Landray MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical trial results in context: comparison of baseline characteristics and outcomes of 38,510 RECOVERY trial participants versus a reference population of 346,271 people hospitalised with COVID-19 in England.</name><description>&lt;h4>Background&lt;/h4>Randomised trials are essential to reliably assess medical interventions. Nevertheless, interpretation of such studies, particularly when considering absolute effects, is enhanced by understanding how the trial population may differ from the populations it aims to represent.&lt;h4>Methods&lt;/h4>We compared baseline characteristics and mortality of RECOVERY participants recruited in England (n = 38,510) with a reference population hospitalised with COVID-19 in England (n = 346,271) from March 2020 to November 2021. We used linked hospitalisation and mortality data for both cohorts to extract demographics, comorbidity/frailty scores, and crude and age- and sex-adjusted 28-day all-cause mortality.&lt;h4>Results&lt;/h4>Demographics of RECOVERY participants were broadly similar to the r</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-07-15T10:00:09.902Z</modification><creation>2025-04-04T12:21:08.545Z</creation></dates><accession>S-EPMC11218071</accession><cross_references><pubmed>38951929</pubmed><doi>10.1186/s13063-024-08273-9</doi></cross_references></HashMap>