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Ivabradine vs Placebo: All-cause of Mortality

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.1040.09660.113wilsonClinicalTrials.gov
Risk in group 20.1010.09290.109wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.00381-0.007580.0152newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.040.9291.16logClinicalTrials.gov
Odds ratio, group 1 over group 21.040.9211.18logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Ivabradine than on Placebo262from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1IvabradinePatients received ivabradine at starting dose of 5 mg twice daily, with a target dose, if HR tolerance criteria were met after two weeks (at the D15 visit), of 7.5 mg twice daily.5725,479OG000ClinicalTrials.gov
Group 2PlaceboPatients received placebo twice daily.5475,438OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleAll-cause of MortalityClinicalTrials.gov
DescriptionClinicalTrials.gov
Time frameFrom the date of randomisation to death, up to 3 years.ClinicalTrials.gov
PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleThe BEAUTIFUL Study: Effects of Ivabradine in Patients With Stable Coronary Artery Disease and Left Ventricular Systolic DysfunctionClinicalTrials.gov
NCT numberNCT00143507ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsCoronary Disease, Ventricular Dysfunction, LeftClinicalTrials.gov
InterventionsIvabradine, PlaceboClinicalTrials.gov
Lead sponsorInstitut de Recherches Internationales ServierClinicalTrials.gov
Results first posted2015-06-25ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00143507?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.