Comparison · NCT01380782-sae
Arm A vs Arm B: 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 A vs Arm B: serious adverse events. Trial comparisons, record NCT01380782-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01380782-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 | 0.364 | 0.197 | 0.57 | wilson | |
| Risk in group 2 | 0.357 | 0.163 | 0.612 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00649 | -0.298 | 0.29 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.02 | 0.416 | 2.49 | log | |
| Odds ratio, group 1 over group 2 | 1.03 | 0.255 | 4.16 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Arm A than on Arm B | 154 | 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 | Arm A | Bevacizumab-naive participants | 8 | 22 | EG000 |
| Group 2 | Arm B | Bevacizumab-treated participants | 5 | 14 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse events were collected on each participant from the time the informed consent document was signed up until 30 days after the last dose of study drug.
Source ClinicalTrials.gov
Trial
- Title
- BIBF 1120 for Recurrent High-Grade Gliomas
- NCT number
- NCT01380782
- Phases
- PHASE2
- Conditions
- Glioblastoma, Gliosarcoma, Anaplastic Astrocytoma, Anaplastic Oligodendroglioma, Anaplastic Oligoastrocytoma
- Interventions
- BIBF 1120
- Lead sponsor
- Patrick Y. Wen, MD
- Results first posted
- 2014-08-18
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01380782?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.
For software
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GET https://conductscience.org/api/comparisons/v1/NCT01380782-sae