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Comparison · NCT00092677-307b746c

EZ/Simva 10/40 mg vs Placebo: Hospitalization for Unstable Angina

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. EZ/Simva 10/40 mg vs Placebo: Hospitalization for Unstable Angina. Trial comparisons, record NCT00092677-307b746c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00092677-307b746c

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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 10.00530.002260.0123wilson
Risk in group 20.008610.004370.0169wilson
Risk difference, group 1 minus group 2-0.00331-0.01210.00491newcombe hybrid score
Risk ratio, group 1 over group 20.6150.2021.87log
Odds ratio, group 1 over group 20.6130.21.88log
Number needed to treat, for one fewer participant with the outcome on EZ/Simva 10/40 mg than on Placebo302from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1EZ/Simva 10/40 mgEzetimibe 10 mg + Simvastatin 40 mg5944OG000
Group 2Placebo8929OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Hospitalization for Unstable Angina
Description
Number of participants that experienced hospitalization for unstable angina
Time frame
Entire follow-up (median = 4.35 years)
Population
Intention-to-Treat

Source ClinicalTrials.gov

Trial

Title
An Investigational Drug on Clinical Outcomes in Patients With Aortic Stenosis (Narrowing of the Major Blood Vessel of the Heart)(MK-0653A-043 AM4)(COMPLETED)
NCT number
NCT00092677
Phases
PHASE3
Conditions
Aortic Stenosis
Interventions
ezetimibe (+) simvastatin, Comparator: Placebo
Lead sponsor
Organon and Co
Results first posted
2009-05-27

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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