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Dapa 10 mg vs Placebo: deaths from any cause

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 10.1630.150.176wilsonClinicalTrials.gov
Risk in group 20.170.1570.184wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00729-0.02570.0112newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9570.8571.07logClinicalTrials.gov
Odds ratio, group 1 over group 20.9490.8311.08logClinicalTrials.gov
Number needed to treat, for one fewer death from any cause on Dapa 10 mg than on Placebo137from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Dapa 10 mgDapagliflozin 10 mg tablets administered once daily per oral use5103,131EG000ClinicalTrials.gov
Group 2PlaceboPlacebo tablet to match dapagliflozin 10 mg, given once daily per oral use5333,132EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, all-cause mortalityClinicalTrials.gov
Time frame[All-cause mortality]: From randomization until end of study, up to 42.2 months. [Serious AE and other AE] From first dose until end of study, up to 42.2 months.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleDapagliflozin Evaluation to Improve the LIVEs of Patients With PReserved Ejection Fraction Heart Failure.ClinicalTrials.gov
NCT numberNCT03619213ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsHeart Failure With Preserved Ejection FractionClinicalTrials.gov
InterventionsDapagliflozin, PlaceboClinicalTrials.gov
Lead sponsorAstraZenecaClinicalTrials.gov
Results first posted2023-07-11ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT03619213?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.