<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Bishop C</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4> This double-blind RCT investigated raising serum 25-hydroxyvitamin D (25D) with extended-release calcifediol (ERC) on time to symptom resolution in mild to moderate COVID-19. &lt;h4>Research Methods &amp; Procedures&lt;/h4> COVID-19 outpatients received oral ERC (300 mcg on Days 1-3 and 60 mcg on Days 4-27) or placebo (NCT04551911). Symptoms were self-reported daily. Primary endpoints were raising 25D to ≥50 ng/mL and decreasing resolution time for five aggregated symptoms (three respiratory). &lt;h4>Results&lt;/h4> 171 subjects were randomized, 160 treated and 134 (65 ERC, 69 placebo) retained. Average age was 43 (range: 18-71), 59% female, mean baseline 25D was 37±1 (SE) ng/mL. In the full analysis set (FAS), 81% of ERC subjects achieved 25D levels of ≥50 ng/mL versus 15% with placebo</pubmed_abstract><journal>Nutrition (Burbank, Los Angeles County, Calif.)</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9639413</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>REsCue Trial: Randomized Controlled Clinical Trial with Extended-Release Calcifediol in Symptomatic COVID-19 Outpatients</pubmed_title><pmcid>PMC9639413</pmcid><pubmed_authors>Federman N</pubmed_authors><pubmed_authors>Strugnell S</pubmed_authors><pubmed_authors>Kalantar-Zadeh K</pubmed_authors><pubmed_authors>Bishop C</pubmed_authors><pubmed_authors>Vazquez-Escarpanter E</pubmed_authors><pubmed_authors>Choe J</pubmed_authors><pubmed_authors>Melnick J</pubmed_authors><pubmed_authors>Ng D</pubmed_authors><pubmed_authors>Ashfaq A</pubmed_authors><pubmed_authors>Adams J</pubmed_authors><pubmed_authors>Fialkow J</pubmed_authors></additional><is_claimable>false</is_claimable><name>REsCue Trial: Randomized Controlled Clinical Trial with Extended-Release Calcifediol in Symptomatic COVID-19 Outpatients</name><description>&lt;h4>Objective&lt;/h4> This double-blind RCT investigated raising serum 25-hydroxyvitamin D (25D) with extended-release calcifediol (ERC) on time to symptom resolution in mild to moderate COVID-19. &lt;h4>Research Methods &amp; Procedures&lt;/h4> COVID-19 outpatients received oral ERC (300 mcg on Days 1-3 and 60 mcg on Days 4-27) or placebo (NCT04551911). Symptoms were self-reported daily. Primary endpoints were raising 25D to ≥50 ng/mL and decreasing resolution time for five aggregated symptoms (three respiratory). &lt;h4>Results&lt;/h4> 171 subjects were randomized, 160 treated and 134 (65 ERC, 69 placebo) retained. Average age was 43 (range: 18-71), 59% female, mean baseline 25D was 37±1 (SE) ng/mL. In the full analysis set (FAS), 81% of ERC subjects achieved 25D levels of ≥50 ng/mL versus 15% with placebo</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-05T11:27:24.719Z</modification><creation>2025-04-05T11:27:24.719Z</creation></dates><accession>S-EPMC9639413</accession><cross_references/></HashMap>