Comparison · NCT02540993-5a39d043
Finerenone vs Placebo: All-cause Hospitalization
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. Finerenone vs Placebo: All-cause Hospitalization. Trial comparisons, record NCT02540993-5a39d043. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02540993-5a39d043
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.446 | 0.428 | 0.464 | wilson | |
| Risk in group 2 | 0.465 | 0.447 | 0.483 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0192 | -0.045 | 0.00675 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.959 | 0.906 | 1.01 | log | |
| Odds ratio, group 1 over group 2 | 0.926 | 0.834 | 1.03 | log | |
| Number needed to treat, for one fewer participant with the outcome on Finerenone than on Placebo | 52.2 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Finerenone | Participants received finerenone 10 mg or 20 mg once daily in addition to standard of care therapy | 1,263 | 2,833 | OG000 |
| Group 2 | Placebo | Participants received matching placebo once daily in addition to standard of care therapy | 1,321 | 2,841 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- All-cause Hospitalization
- Description
Count of participants and time from randomization to the first occurrence of a hospitalization event were evaluated. Number of participants with the event is reported as descriptive result and hazard ratio is reported as statistical analysis.
- Time frame
- From randomization up until the first occurrence of the hospitalization due to any cause, or censoring at the end of study, with an average of 32 months
- Population
- Full analysis set
Source ClinicalTrials.gov
Trial
- Title
- Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease
- NCT number
- NCT02540993
- Phases
- PHASE3
- Conditions
- Chronic Kidney Disease
- Interventions
- Finerenone (BAY94-8862), Placebo
- Lead sponsor
- Bayer
- Results first posted
- 2021-07-19
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02540993?tab=results
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.govNone 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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