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Home   COVID-19 treatment studies for Vitamin D  COVID-19 treatment studies for Vitamin D  C19 studies: Vitamin D  Vitamin D   Select treatmentSelect treatmentTreatmentsTreatments
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All Studies   Meta Analysis   Recent: 
0 0.5 1 1.5 2+ Mortality -44% Improvement Relative Risk ICU admission -5% Hospitalization time -5% no CI Mortality (b) -117% levels ICU admission (b) 65% levels Progression 79% levels c19vitamind.com Cannata-Andía et al. NCT04552951 Vitamin D RCT LATE Favors vitamin D Favors control
Cannata-Andía, 543 patient vitamin D late treatment RCT: 44% higher mortality [p=0.31], 5% higher ICU admission [p=0.82], 5% higher hospitalization, and 79% lower progression [p=0.003] https://c19p.org/cannataandia
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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
Cannata-Andía et al., BMC Medicine, doi:10.1186/s12916-022-02290-8
18 Feb 2022    Source   PDF   Share   Tweet
RCT 274 very late stage (>80% pulmonary involvement at baseline) hospitalized COVID-19 patients treated with a single dose of cholecalciferol, and 269 control patients, showing no significant differences. High serum calcidiol levels at admission were associated with lower pulmonary involvement, shorter hospitalization, and lower ICU admission.
Serum levels increased in the treatment group, however average levels were still insufficient at discharge. Calcifediol or calcitriol, which avoids several days delay in conversion, may be more successful, especially with this very late stage usage.
COVID-VIT-D. 100,000IU cholecalciferol. NCT04552951.
risk of death, 44.0% higher, RR 1.44, p = 0.31, treatment 22 of 274 (8.0%), control 15 of 269 (5.6%).
risk of ICU admission, 4.9% higher, RR 1.05, p = 0.82, treatment 47 of 274 (17.2%), control 44 of 269 (16.4%).
hospitalization time, 5.3% higher, relative time 1.05, treatment 274, control 269.
risk of death, 117.0% higher, RR 2.17, p = 0.20, high D levels 87, low D levels 96, >25 vs. ≤10 ng/mL, adjusted by demographics, comorbidities, and laboratory parameters, outcome based on serum levels.
risk of ICU admission, 65.0% lower, RR 0.35, p = 0.04, high D levels 87, low D levels 96, >25 vs. ≤10 ng/mL, adjusted by demographics, comorbidities, and laboratory parameters, outcome based on serum levels.
risk of progression, 79.0% lower, RR 0.21, p = 0.003, high D levels 87, low D levels 96, pulmonary involvment at admission, >25 vs. ≤10 ng/mL, adjusted by demographics, comorbidities, and laboratory parameters, outcome based on serum levels.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
This study is excluded in the after exclusion results of meta analysis: very late stage study using cholecalciferol instead of calcifediol or calcitriol.
Cannata-Andía et al., 2/18/2022, Randomized Controlled Trial, multiple countries, multiple regions, peer-reviewed, median age 59.0, 22 authors, dosage 100,000IU single dose, trial NCT04552951.
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Late treatment
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