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Comparison · NCT04333732-7d39caf8

M-M-R II ® vs Placebo: Severity of COVID-19 Measured at 60 Days After Intervention

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. M-M-R II ® vs Placebo: Severity of COVID-19 Measured at 60 Days After Intervention. Trial comparisons, record NCT04333732-7d39caf8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04333732-7d39caf8

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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 10.001870.0006350.00547wilson
Risk in group 20.0006480.0001140.00366wilson
Risk difference, group 1 minus group 20.00122-0.002030.00487newcombe hybrid score
Risk ratio, group 1 over group 22.880.327.7log
Odds ratio, group 1 over group 22.890.327.8log
Number needed to treat, for one more participant with the outcome on M-M-R II ® than on Placebo820from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1M-M-R II ®Education and surveillance plus M-M-R II ® Single dose, 0.5 mL subcutaneous injection of M-M-R II ®~MR or M-M-R II ® vaccine: Education and surveillance plus MR or M-M-R II ® vaccine31,607OG000
Group 2PlaceboEducation and surveillance plus placebo Single dose, 0.5 mL subcutaneous injection of 0.9% saline~Placebo: Placebo injection11,544OG001

Outcome

Type
SECONDARY
Title
Severity of COVID-19 Measured at 60 Days After Intervention
Description
Severity of COVID-19 in adults who become infected with SARS-CoV-2 by day 60 after receiving trial intervention. Severity will be graded on a simplified version of the ordinal WHO COVID-19 severity scale ((i) uninfected, (ii) infected but ambulatory \[mild disease\], (iii) infected and hospitalized \[moderate or severe disease\] or dead). Practically, this outcome measure was treated as a binary outcome - participants were classified and counted as having severe COVID-19 if they met the definition for the primary outcome of symptomatic COVID-19 AND were hospitalized during the course of their COVID-19 illness.
Time frame
60 days after receiving trial intervention
Population

Source ClinicalTrials.gov

Trial

Title
CROWN CORONATION: COVID-19 Research Outcomes Worldwide Network for CORONAvirus prevenTION
NCT number
NCT04333732
Phases
PHASE3
Conditions
COVID 19
Interventions
MR or M-M-R II ® vaccine, Placebo
Lead sponsor
Washington University School of Medicine
Results first posted
2024-03-26

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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