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Trial · NCT02139046

Adverse event totals15

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo
Total, all-cause mortalityFebuxostat IR 40 mg
Total, all-cause mortalityFebuxostat XR 40 mg
Total, all-cause mortalityFebuxostat IR 80 mg
Total, all-cause mortalityFebuxostat XR 80 mg
Total, other adverse eventsPlacebo53356
Total, other adverse eventsFebuxostat IR 40 mg53358
Total, other adverse eventsFebuxostat XR 40 mg45355
Total, other adverse eventsFebuxostat IR 80 mg55357
Total, other adverse eventsFebuxostat XR 80 mg38357
Total, serious adverse eventsPlacebo8356
Total, serious adverse eventsFebuxostat IR 40 mg12358
Total, serious adverse eventsFebuxostat XR 40 mg6355
Total, serious adverse eventsFebuxostat IR 80 mg8357
Total, serious adverse eventsFebuxostat XR 80 mg8357

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

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/NCT02139046/event-totals