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Trial · NCT01331837

Outcomes18

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTime to First Cardiovascular (CV) Events Adjudication Committee (EAC) (CV-EAC) Adjudicated EventFrom baseline up to 4.9 yearsAnalysis was conducted on the Intention to treat (ITT) population, i.e. all patients randomized who have taken at least one dose of study medicationMonthsMEDIAN
PRIMARYPercentage of Patients Reporting a Cardiovascular (CV) Events Adjudication Committee (EAC) (CV-EAC) Adjudicated EventFrom baseline up to 4.9 yearsAnalysis was conducted on the Intention to treat (ITT) population, i.e. all patients randomized who have taken at least one dose of study medicationPercentage of patients with eventNUMBER
PRIMARYTime to First CV-EAC Adjudicated Event - Sensitivity AnalysisFrom Baseline up to 4.9 yearsAnalyses was conducted on the On-treatment (OT) population, i.e. patients who switched from randomized treatment were censored at the time of treatment switching.MonthsMEDIAN
PRIMARYPercentage of Patients With a CV-EAC Adjudicated Event - Sensitivity AnalysisFrom Baseline up to 4.9 yearsAnalyses was conducted on the On-treatment (OT) population, i.e. patients who switched from randomized treatment were censored at the time of treatment switching.Percentage of patients with eventNUMBER
PRIMARYTime to First CV-EAC Adjudicated Event Excluding Undetermined Cause of Death - Sensitivity AnalysisFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT populationMonthsMEDIAN
PRIMARYPercentage of Patients With a CV-EAC Adjudicated Event Excluding Undetermined Cause of Death - Sensitivity AnalysisFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT populationPercentage of patients with eventNUMBER
PRIMARYTime to First CV-EAC Adjudicated Event Before Last Direct Contact DateFrom Baseline up to 4.9 yearsAnalysis was conducted on the ITT populationMonthsMEDIAN
PRIMARYPercentage of Participants With a CV-EAC Adjudicated Event Before Last Direct Contact DateFrom Baseline up to 4.9 yearsAnalysis was conducted on the ITT populationPercentage of participants with eventNUMBER
SECONDARYThe Time to First Occurrence of an Expanded CV Composite EndpointFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT population.MonthsMEDIAN
SECONDARYPercentages of Participants With an Expanded CV Composite EndpointFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT population.Percentages of participantsNUMBER
SECONDARYTime to First Occurrence of Individual Component of Primary Endpoint: Non-fatal Myocardial InfarctionFrom baseline up to 4.9 yearsAnlysis was conducted on the ITT population.MonthsMEDIAN
SECONDARYPercentage of Patients With Individual Component of Primary Endpoint: Non-fatal Myocardial InfarctionFrom baseline up to 4.9 yearsAnlysis was conducted on the ITT populationPercentage of patientsNUMBER
SECONDARYTime to First Occurrence of Individual Component of Primary Endpoint: Cardiovascular DeathFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT populationMonthsMEDIAN
SECONDARYPercentage of Patients With Individual Component of Primary Endpoint: Cardiovascular DeathFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT populationPercentage of patientsNUMBER
SECONDARYTime to First Occurrence of Individual Component of Primary Endpoint: Non-fatal StrokeFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT populationMonthsMEDIAN
SECONDARYPercentage of Patients With Individual Component of Primary Endpoint: Non-fatal StrokeFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT populationPercentage of patientsNUMBER
SECONDARYTime to First Occurrence of Individual Component of Primary Endpoint: All-cause MortalityFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT population.MonthsMEDIAN
SECONDARYPercentage of Patients With Individual Component of Primary Endpoint: All-cause MortalityFrom baseline up to 4.9 yearsAnalysis was conducted on the ITT population.Percentage of patientsNUMBER

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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GET https://conductscience.org/api/trials/v1/NCT01331837/outcomes