Comparison · NCT02348203-sae
Arm I (Aspirin, Zileuton) vs Arm II (Double 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. Arm I (Aspirin, Zileuton) vs Arm II (Double Placebo): serious adverse events. Trial comparisons, record NCT02348203-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02348203-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 | 0 | 0.11 | wilson | |
| Risk in group 2 | 0 | 0 | 0.107 | wilson | |
| Risk difference, group 1 minus group 2 | 0 | -0.107 | 0.11 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | log | a group has no participants with the outcome | |||
| Odds ratio, group 1 over group 2 | log | a cell of the two-by-two table is zero | |||
| Number needed to harm | from the risk difference interval | the two groups' risks are equal |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Arm I (Aspirin, Zileuton) | Patients receive aspirin PO QD and zileuton PO BID for 12 weeks in the absence of unacceptable toxicity.~Aspirin: Given PO~Laboratory Biomarker Analysis: Correlative studies~Zileuton: Given PO | 0 | 31 | EG000 |
| Group 2 | Arm II (Double Placebo) | Patients receive aspirin placebo PO QD and zileuton placebo PO BID for 12 weeks.~Laboratory Biomarker Analysis: Correlative studies~Placebo Administration: Given aspirin placebo PO~Placebo Administration: Given zileuton placebo PO | 0 | 32 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse event data were collected from the time that the first dose of study drug was taken until 2 weeks after participants come off the 12-week agent intervention.
Source ClinicalTrials.gov
Trial
- Title
- Aspirin and Zileuton and Biomarker Expression in Nasal Tissue of Current Smokers
- NCT number
- NCT02348203
- Phases
- PHASE2
- Conditions
- Tobacco Use Disorder
- Interventions
- Aspirin, Laboratory Biomarker Analysis, Placebo Administration, Placebo Administration, Zileuton
- Lead sponsor
- National Cancer Institute (NCI)
- Results first posted
- 2020-03-23
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02348203?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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