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Trial · NCT00174941

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityFebuxostat 40 mg QD
Total, all-cause mortalityFebuxostat 80 mg QD
Total, all-cause mortalityFebuxostat 120 mg QD
Total, all-cause mortalityFebuxostat Total
Total, other adverse eventsFebuxostat 40 mg QD512
Total, other adverse eventsFebuxostat 80 mg QD44116
Total, other adverse eventsFebuxostat 120 mg QD937
Total, other adverse eventsFebuxostat Total53116
Total, serious adverse eventsFebuxostat 40 mg QD312
Total, serious adverse eventsFebuxostat 80 mg QD14116
Total, serious adverse eventsFebuxostat 120 mg QD437
Total, serious adverse eventsFebuxostat Total21116

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/NCT00174941/event-totals