Comparison · NCT00786643-sae
Stratum 1 vs Stratum 2: 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. Stratum 1 vs Stratum 2: serious adverse events. Trial comparisons, record NCT00786643-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00786643-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 | 0.1 | 0.0279 | 0.301 | wilson | |
| Risk in group 2 | 0.185 | 0.0818 | 0.367 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0852 | -0.281 | 0.141 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.54 | 0.116 | 2.51 | log | |
| Odds ratio, group 1 over group 2 | 0.489 | 0.0846 | 2.83 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Stratum 1 than on Stratum 2 | 11.7 | 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 | Stratum 1 | Patients in stratum 1 have not received prior chemotherapy in the metastatic setting. | 2 | 20 | EG000 |
| Group 2 | Stratum 2 | Patients in stratum 2 have received 1-2 prior chemotherapy regimens in the metastatic setting. | 5 | 27 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse events were collected beginning on day 1 of study treatment until one month after the end of study treatment (approximately every 14 days for up to 310 days).
Source ClinicalTrials.gov
Trial
- Title
- Study of Gamma Interfereon in Metastatic Colorectal Carcinoma
- NCT number
- NCT00786643
- Phases
- PHASE2
- Conditions
- Colorectal Cancer
- Interventions
- 5-Fluorouracil, Leucovorin (LV), Gamma-Interferon-1b (IFN-γ), Bevacizumab
- Lead sponsor
- Accelerated Community Oncology Research Network
- Results first posted
- 2012-02-22
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00786643?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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GET https://conductscience.org/api/comparisons/v1/NCT00786643-sae