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Trial · NCT00385138

Outcomes20

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYIncidence of All-cause Mortality, Myocardial Infarction (MI), and Ischemia-driven Revascularization (IDR)randomization through 48 hours post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of All-cause Mortality or MIrandomization through 48 hours post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of All-cause Mortalityrandomization through 48 hours post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of MIrandomization through 48 hours post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of IDRrandomization through 48 hours post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of Stent Thrombosisrandomization through 48 hours post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of Strokerandomization through 48 hours post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of All-cause Mortalityrandomization through 1 year post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARY
Incidence of Procedure Events [Abrupt Closure, Threatened Abrupt Closure, Need for Urgent Coronary Artery Bypass Graft (CABG) Surgery, Unsuccessful Procedure, New Thrombus or Suspected Thrombus, and/or Acute Stent Thrombosis]
During index PCImITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of GUSTO Severe / Life-threateningrandomization through 48 hours post randomizationSafety populationparticipantsNUMBER
SECONDARYIncidence of Thrombolysis in Myocardial Infarction (TIMI) Majorrandomization through 48 hours post randomizationSafety populationparticipantsNUMBER
SECONDARYIncidence of ACUITY Major Bleedingrandomization through 48 hours post randomizationSafety populationparticipantsNUMBER
SECONDARYIncidence of ACUITY Major Bleeding Without Hematoma >/= 5 cmrandomization through 48 hours post randomizationSafety populationparticipantsNUMBER
SECONDARYIncidence of All-cause Mortality, MI, or IDRrandomization through 30 days post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of All-cause Mortality or MIrandomization through 30 days post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of All-cause Mortalityrandomization through 30 days post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of MIrandomization through 30 days post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of IDRrandomization through 30 days post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of Stent Thrombosisrandomization through 30 days post randomizationmITT population, based on available dataparticipantsNUMBER
SECONDARYIncidence of Strokerandomization through 30 days post randomizationmITT population, based on available dataparticipantsNUMBER

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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