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Comparison · NCT04344184-deaths

Infusion vs Placebo: deaths from any cause

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Infusion vs Placebo: deaths from any cause. Trial comparisons, record NCT04344184-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04344184-deaths

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.2270.1010.434wilson
Risk in group 20.280.1430.476wilson
Risk difference, group 1 minus group 2-0.0527-0.2860.196newcombe hybrid score
Risk ratio, group 1 over group 20.8120.32.19log
Odds ratio, group 1 over group 20.7560.2012.85log
Number needed to treat, for one fewer death from any cause on Infusion than on Placebo19from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1InfusionL-Ascorbic Acid (Vitamin C), intravenous infusion~L-ascorbic acid: 50 mg/kg intravenous vitamin C infusion every 6 hours for up to 96 hours522EG000
Group 2PlaceboDextrose 5% Water~Placebo: Dextrose 5% Water725EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse events were monitored/assessed from baseline to the end of study procedures, or until participants withdrew from the study, up to day 90 for each enrolled participant

Source ClinicalTrials.gov

Trial

Title
SAFEty Study of Early Infusion of Vitamin C for Treatment of Novel Coronavirus Acute Lung Injury (SAFE EVICT CORONA-ALI)
NCT number
NCT04344184
Phases
PHASE2
Conditions
COVID-19, Lung Injury, Acute, Kidney Injury
Interventions
L-ascorbic acid, Placebo
Lead sponsor
Virginia Commonwealth University
Results first posted
2024-04-04

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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