ConductScience.org, home

Trial · NCT02247245

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo013
Total, all-cause mortalityIvabradine013
Total, all-cause mortalityAtrial Fibrillation (Low Rate)07
Total, all-cause mortalityAtrial Fibrilaltion (Standard Rate)07
Total, other adverse eventsPlacebo013
Total, other adverse eventsIvabradine013
Total, other adverse eventsAtrial Fibrillation (Low Rate)07
Total, other adverse eventsAtrial Fibrilaltion (Standard Rate)07
Total, serious adverse eventsPlacebo013
Total, serious adverse eventsIvabradine013
Total, serious adverse eventsAtrial Fibrillation (Low Rate)07
Total, serious adverse eventsAtrial Fibrilaltion (Standard Rate)07

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/NCT02247245/event-totals