Comparison · NCT01496469-sae
Febuxostat 80 mg vs Placebo: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Febuxostat 80 mg vs Placebo: serious adverse events. Trial comparisons, record NCT01496469-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01496469-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0164 | 0.0029 | 0.0872 | wilson | |
| Risk in group 2 | 0.0167 | 0.00295 | 0.0886 | wilson | |
| Risk difference, group 1 minus group 2 | -0.000273 | -0.0734 | 0.0718 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.984 | 0.063 | 15.4 | log | |
| Odds ratio, group 1 over group 2 | 0.983 | 0.0601 | 16.1 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Febuxostat 80 mg than on Placebo | 3,660 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Febuxostat 80 mg | Febuxostat 80 mg, over-encapsulated tablet, orally, once daily for up to 6 week. | 1 | 61 | EG001 |
| Group 2 | Placebo | Febuxostat placebo-matching over-encapsulated tablet, orally, once daily for up to 6 weeks. | 1 | 60 | EG000 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Treatment-emergent AEs are defined as any AEs, regardless of relationship to study drug, which occurs on or after the first double-blind dose date and up to 30 days after the last dose date of the double-blind study drug.
Source ClinicalTrials.gov
Trial
- Title
- Effect of Febuxostat on Blood Pressure
- NCT number
- NCT01496469
- Phases
- PHASE2
- Conditions
- Hypertension
- Interventions
- Febuxostat, Placebo
- Lead sponsor
- Takeda
- Results first posted
- 2015-08-31
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01496469?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
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
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
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