Ivabradine vs Placebo: Secondary Composite Endpoint
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.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note | Source |
|---|---|---|---|---|---|---|
| Risk in group 1 | 0.255 | 0.24 | 0.27 | wilson | ClinicalTrials.gov | |
| Risk in group 2 | 0.3 | 0.284 | 0.316 | wilson | ClinicalTrials.gov | |
| Risk difference, group 1 minus group 2 | -0.0454 | -0.0671 | -0.0236 | newcombe hybrid score | ClinicalTrials.gov | |
| Risk ratio, group 1 over group 2 | 0.849 | 0.784 | 0.918 | log | ClinicalTrials.gov | |
| Odds ratio, group 1 over group 2 | 0.797 | 0.715 | 0.889 | log | ClinicalTrials.gov | |
| Number needed to treat, for one fewer participant with the outcome on Ivabradine than on Placebo | 22 | 14.9 | 42.3 | from the risk difference interval | ClinicalTrials.gov |
Groups 2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code | Source |
|---|---|---|---|---|---|---|
| Group 1 | Ivabradine | Ivabradine: 2.5mg, 5mg or 7.5mg tablets to be taken orally twice daily, at 12-hours intervals, in the morning and in the evening during meals up to 42 months. | 825 | 3,241 | OG000 | ClinicalTrials.gov |
| Group 2 | Placebo | Placebo: Matching placebo tablets to be taken orally twice daily, at 12-hours intervals, in the morning and in the evening during meals up to 42 months. | 979 | 3,264 | OG001 | ClinicalTrials.gov |
Outcome 5
| Field | Value | Source |
|---|---|---|
| Type | SECONDARY | ClinicalTrials.gov |
| Title | Secondary Composite Endpoint | ClinicalTrials.gov |
| Description | CV death, hospitalisation for worsening HF or hospitalisation for non-fatal myocardial infarction | ClinicalTrials.gov |
| Time frame | From the date of randomisation to the date of the first event, up to 42 months | ClinicalTrials.gov |
| Population | ClinicalTrials.gov |
Trial 8
| Field | Value | Source |
|---|---|---|
| Title | Effects of Ivabradine on Cardiovascular Events in Patients With Moderate to Severe Chronic Heart Failure and Left Ventricular Systolic Dysfunction. A Three-year International Multicentre Study | ClinicalTrials.gov |
| NCT number | NCT02441218 | ClinicalTrials.gov |
| Phases | PHASE3 | ClinicalTrials.gov |
| Conditions | Chronic Heart Failure | ClinicalTrials.gov |
| Interventions | Ivabradine, Placebo | ClinicalTrials.gov |
| Lead sponsor | Institut de Recherches Internationales Servier | ClinicalTrials.gov |
| Results first posted | 2015-06-29 | ClinicalTrials.gov |
| Results on ClinicalTrials.gov | https://clinicaltrials.gov/study/NCT02441218?tab=results | ClinicalTrials.gov |
Source 4
| Field | Value | Source |
|---|---|---|
| Release | trial-comparisons-2026-03-23-0.1.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57 | ClinicalTrials.gov |
| AACT copy | 2026-03-23 | ClinicalTrials.gov |
| 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 | ClinicalTrials.gov |
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.