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Trial · NCT00808067

Outcomes14

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMajor Bleeding, Annualized Rate of Subjects With Major Bleedsup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYStroke, Annualized Rate of Subjects With Strokeup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYNon CNS Systemic Embolism (SEE), Annualized Rate of Subjects With Non-CNS SEEup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYPulmonary Embolism (PE), Annualized Rate of Subjects With PEup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYAcute Myocardial Infarction (MI), Annualized Rate of Subjects With MIup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYDeep Vein Thrombosis, Annualized Rate of Subjects With DVTup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYDeath, Annualized Rate of Subject Deathup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYAnnualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE)up to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYAnnualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE) and All Cause Deathup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYAnnualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE), Pulmonary Embolism (PE), Myocardial Infarction, Vascular Deathup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYAnnualized Rate of Subjects With Composite Incidence of Stroke, Non CNS Systemic Embolism (SEE), Pulmonary Embolism (PE), Myocardial Infarction (MI), All Cause Death and Major Bleedup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYAnnualized Rate of Subjects With Minor Bleedsup to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYAnnualized Rate of Subjects With Any Bleeds (Major Plus Minor)up to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER
SECONDARYAnnualized Rate of Subjects With Intra-Cranial Hemorrhage (ICH)up to 43 monthsSAF-FAS intervalpercentage of subject-yearsNUMBER

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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