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Trial · NCT00307047

Outcomes66

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

TypeOutcomeTime framePopulationUnitsMeasured as
SECONDARYIschemia Driven Target Vessel Failure (TVF)30 dayspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Failure (TVF)180 dayspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Failure (TVF)270 dayspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Failure (TVF)1 yearITT, @ 1 yrpercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Failure (TVF)2 yearsITT, @ 2 yearspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Failure (TVF)3 yearsITT, @ 3 yearspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Lesion Revascularization (TLR)30 daysITT population.percentage of participantsNUMBER
SECONDARYIschemia Driven Target Lesion Revascularization (TLR)180 daysITT populationpercentage of participantsNUMBER
SECONDARYIschemia Driven Target Lesion Revascularization (TLR)270 daysITT populationpercentage of participantsNUMBER
SECONDARYIschemia Driven Target Lesion Revascularization (TLR)1 yearITT population.percentage of participantsNUMBER
SECONDARYIschemia Driven Target Lesion Revascularization (TLR)2 yearsITT population.percentage of participantsNUMBER
SECONDARYIschemia Driven Target Lesion Revascularization (TLR)3 yearsITT population.percentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Revascularization (TVR)30 dayspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Revascularization (TVR)180 dayspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Revascularization (TVR)270 dayspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Revascularization (TVR)1 yearpercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Revascularization (TVR)2 yearspercentage of participantsNUMBER
SECONDARYIschemia Driven Target Vessel Revascularization (TVR)3 yearspercentage of participantsNUMBER
SECONDARYIschemia Driven Major Adverse Cardiac Events (MACE)30 daysPercentage of participantsNUMBER
SECONDARYIschemia Driven Major Adverse Cardiac Events (MACE)180 daysPercentage of participantsNUMBER

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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