Comparison · NCT01806259-58df8c79
Ketorolac 30 mg vs NaCl 0.9% 3mL: Recurrence-free Survival
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
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ConductScience Library. Ketorolac 30 mg vs NaCl 0.9% 3mL: Recurrence-free Survival. Trial comparisons, record NCT01806259-58df8c79. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01806259-58df8c79
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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 | 0.833 | 0.746 | 0.895 | wilson | |
| Risk in group 2 | 0.897 | 0.825 | 0.942 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0639 | -0.162 | 0.0307 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.929 | 0.832 | 1.04 | log | |
| Odds ratio, group 1 over group 2 | 0.573 | 0.252 | 1.3 | log | |
| Number needed to treat, for one fewer participant with the outcome on Ketorolac 30 mg than on NaCl 0.9% 3mL | 15.7 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Ketorolac 30 mg | Active drug to be compared with placebo~Ketorolac 30 mg IV | 80 | 96 | OG000 |
| Group 2 | NaCl 0.9% 3mL | Ketorolac 30 mg IV | 96 | 107 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- PRIMARY
- Title
- Recurrence-free Survival
- Description
2 years for the primary analysis + 3 additional years for secondary analysis (From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 5 years)
- Time frame
- 5 years
- Population
Source ClinicalTrials.gov
Trial
- Title
- Ketorolac in Breast Cancer Surgery
- NCT number
- NCT01806259
- Phases
- PHASE3
- Conditions
- Curative Breast Cancer Surgery, Inflammatory Positive/Negative Status, Pre Surgical Incision Administration
- Interventions
- Ketorolac 30 mg IV, Placebos
- Lead sponsor
- Université Catholique de Louvain
- Results first posted
- 2020-01-18
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01806259?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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