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Dulaglutide vs Placebo: Number of Participants Who Experienced An Event for Time to First Occurrence After Randomization of Heart Failure Requiring Hospitalization or an Urgent Heart Failure Clinic Visit

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 10.0430.03770.0491wilsonClinicalTrials.gov
Risk in group 20.04560.04020.0518wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0026-0.01070.00553newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9430.7851.13logClinicalTrials.gov
Odds ratio, group 1 over group 20.940.7771.14logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Dulaglutide than on Placebo385from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Dulaglutide1.5 mg Dulaglutide was administered once weekly, subcutaneously2134,949OG001ClinicalTrials.gov
Group 2PlaceboPlacebo was administered once weekly, subcutaneously2264,952OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants Who Experienced An Event for Time to First Occurrence After Randomization of Heart Failure Requiring Hospitalization or an Urgent Heart Failure Clinic VisitClinicalTrials.gov
Description
The time to first occurrence after randomization of heart failure requiring hospitalization or an urgent heart failure clinic visit was evaluated using time-to-event analysis via the Cox proportional hazards regression model where response equals treatment. The number of participants who experienced an event is presented.
ClinicalTrials.gov
Time frameFrom randomization to first occurrence or study completion (Median Follow-Up of 5.4 Years)ClinicalTrials.gov
PopulationAll randomized participants.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleResearching Cardiovascular Events With a Weekly Incretin in Diabetes (REWIND)ClinicalTrials.gov
NCT numberNCT01394952ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsCardiovascular Disease, Diabetes Mellitus, Type 2ClinicalTrials.gov
InterventionsDulaglutide, PlaceboClinicalTrials.gov
Lead sponsorEli Lilly and CompanyClinicalTrials.gov
Results first posted2019-10-08ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01394952?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.