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Clopidogrel + ASA vs Placebo + ASA: Death From Any Cause (Cardiovascular and Noncardiovascular)

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 10.2190.2060.232wilsonClinicalTrials.gov
Risk in group 20.2220.2090.236wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00365-0.02230.015newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9840.9041.07logClinicalTrials.gov
Odds ratio, group 1 over group 20.9790.8781.09logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Clopidogrel + ASA than on Placebo + ASA274from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Clopidogrel + ASAClopidogrel 75 mg once daily (od) plus acetylsalicyclic acid (ASA) 75 to 100 mg od recommended (dose at the investigators' discretion)8253,772OG000ClinicalTrials.gov
Group 2Placebo + ASAMatching placebo of clopidogrel 75 mg od plus ASA 75 to 100 mg od recommended (dose at the investigators' discretion)8413,782OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleDeath From Any Cause (Cardiovascular and Noncardiovascular)ClinicalTrials.gov
Description
The considered event is death from any cause. The analysis is performed on the time from randomization to this event. Numbers of patients with the event over the duration of the follow-up are presented by arm group.
ClinicalTrials.gov
Time frameexpected median follow-up of approximately 3 yearsClinicalTrials.gov
PopulationThe intent-to-treat (ITT) population was used for the analysis.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleAtrial Fibrillation Clopidogrel Trial With Irbesartan for Prevention of Vascular Events (ACTIVE A)ClinicalTrials.gov
NCT numberNCT00249873ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsAtrial Fibrillation, Vascular RiskClinicalTrials.gov
Interventionsclopidogrel (SR25990C), placeboClinicalTrials.gov
Lead sponsorSanofiClinicalTrials.gov
Results first posted2010-03-26ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00249873?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.