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Trial · NCT02128490

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 eventsPlacebo338
Total, other adverse eventsFebuxostat IR 40 mg537
Total, other adverse eventsFebuxostat XR 40 mg439
Total, other adverse eventsFebuxostat IR 80 mg137
Total, other adverse eventsFebuxostat XR 80 mg338
Total, serious adverse eventsPlacebo038
Total, serious adverse eventsFebuxostat IR 40 mg137
Total, serious adverse eventsFebuxostat XR 40 mg139
Total, serious adverse eventsFebuxostat IR 80 mg037
Total, serious adverse eventsFebuxostat XR 80 mg438

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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT02128490/event-totals