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Comparison · NCT04508023-ce37f324

Rivaroxaban 10 Milligrams (mg) vs Placebo: Number of Participants Who Were Hospitalized or Dead on Day 35

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. Rivaroxaban 10 Milligrams (mg) vs Placebo: Number of Participants Who Were Hospitalized or Dead on Day 35. Trial comparisons, record NCT04508023-ce37f324. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04508023-ce37f324

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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 10.00780.003340.0181wilson
Risk in group 20.004670.001590.0136wilson
Risk difference, group 1 minus group 20.00313-0.006880.0139newcombe hybrid score
Risk ratio, group 1 over group 21.670.4016.97log
Odds ratio, group 1 over group 21.680.3997.05log
Number needed to treat, for one more participant with the outcome on Rivaroxaban 10 Milligrams (mg) than on Placebo319from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Rivaroxaban 10 Milligrams (mg)
Eligible participants with symptomatic coronavirus disease 2019 (COVID-19) who were at risk of venous and arterial thrombotic complications, received rivaroxaban 10 mg, orally, once daily throughout the 35 days of double-blind treatment period along with ongoing standard of care medications for COVID-19 at the discretion of the treating physician.
5641OG000
Group 2Placebo
Eligible participants with symptomatic COVID-19 who were at risk of venous and arterial thrombotic complications, received placebo matching to rivaroxaban, orally, once daily throughout the 35 days of double-blind treatment period along with ongoing standard of care medications for COVID-19 at the discretion of the treating physician.
3643OG001

Outcome

Type
SECONDARY
Title
Number of Participants Who Were Hospitalized or Dead on Day 35
Description
Number of participants who were hospitalized or dead on Day 35 were reported.
Time frame
At Day 35 (+/- 6 days)
Population
ITT analysis set included all randomized participants who provided informed consent.

Source ClinicalTrials.gov

Trial

Title
A Study of Rivaroxaban to Reduce the Risk of Major Venous and Arterial Thrombotic Events, Hospitalization and Death in Medically Ill Outpatients With Acute, Symptomatic Coronavirus Disease 2019 (COVID-19) Infection
NCT number
NCT04508023
Phases
PHASE3
Conditions
Coronavirus Disease 2019 (COVID-19)
Interventions
Rivaroxaban, Placebo, Standard of Care (SOC)
Lead sponsor
Janssen Research & Development, LLC
Results first posted
2023-07-18

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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