ConductScience.org, home

Trial · NCT02879448

Outcomes11

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARY
Primary Safety Endpoint: Composite Endpoint Rate of Procedure-related Complications, or All-cause Death or Major Bleeding (Defined as Type 3 or Greater Based on the Bleeding Academic Research Consortium (BARC) Definition) (Non-inferiority Analysis)
At 12-monthsThe number of participants analyzed includes subjects who were available at that time of analysisPercentage of participantsNUMBER
PRIMARYPrimary Effectiveness Endpoint: Composite Rate of Ischemic Stroke or Systemic Embolism (Non-inferiority Analysis)At 18-monthsThe number of participants analyzed includes subjects who were available at that time of analysisPercentage of participantsNUMBER
PRIMARYMechanism of Action Primary Endpoint: Rate of Device Closure, by the Echocardiography Core Lab (Non-inferiority Analysis)At 45-daysThe number of participants analyzed includes subjects who were available at that time of analysisPercentage of participantsNUMBER
SECONDARYComposite Rate of All Stroke, Systemic Embolism, or Cardiovascular/Unexplained Death (Non-inferiority Analysis)At 18-monthsThe number of participants analyzed includes subjects who were available at that time of analysisPercentage of participantsNUMBER
SECONDARYRate of Major Bleeding (Superiority Analysis)At 18-monthsThe number of participants analyzed includes subjects who were available at that time of analysisPercentage of participantsNUMBER
SECONDARY
Superiority Test of Primary Safety Endpoint: Composite Endpoint Rate of Procedure-related Complications, or All-cause Death or Major Bleeding (Defined as Type 3 or Greater Based on the Bleeding Academic Research Consortium (BARC) Definition)
At 12-monthsThe number of participants analyzed includes subjects who were available at that time of analysispercentage of participantsNUMBER
SECONDARYSuperiority Test of Primary Effectiveness Endpoint: Composite Rate of Ischemic Stroke or Systemic EmbolismAt 18-monthsThe number of participants analyzed includes subjects who were available at that time of analysisPercentage of participantsNUMBER
SECONDARYSuperiority Test of Primary Mechanism of Action Endpoint: Rate of Device Closure, by the Echocardiography Core LabAt 45-daysThe number of participants analyzed includes subjects who were available at that time of analysisPercentage of participantsNUMBER
POST_HOCComposite Rate of Ischemic Stroke and Systemic Embolism5 YearsAnalysis included subjects who underwent an implant attempt regardless of the device attempted or implanted.percentage of participantsNUMBER
POST_HOCComposite Rate of Stroke, Systemic Embolism, or CV/Unexplained Death5 YearsAnalysis included subjects who underwent an implant attempt regardless of the device attempted or implanted.percentage of participantsNUMBER
POST_HOCRate of Major Bleeding5 YearsAnalysis included subjects who underwent an implant attempt regardless of the device attempted or implanted.percentage 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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT02879448/outcomes