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Comparison · NCT00700102-sae

Chemotherapy vs Chemotherapy + Bevacizumab: serious adverse events

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. Chemotherapy vs Chemotherapy + Bevacizumab: serious adverse events. Trial comparisons, record NCT00700102-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00700102-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.3350.2910.382wilson
Risk in group 20.3240.280.371wilson
Risk difference, group 1 minus group 20.0108-0.05380.0752newcombe hybrid score
Risk ratio, group 1 over group 21.030.8491.26log
Odds ratio, group 1 over group 21.050.7831.41log
Number needed to harm, for one more participant with a serious adverse event on Chemotherapy than on Chemotherapy + Bevacizumab92.8from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1ChemotherapyChemotherapy alone until disease progression, unacceptable toxicity, or patient refusal137409EG000
Group 2Chemotherapy + BevacizumabChemotherapy and Bevacizumab until disease progression, unacceptable toxicity, or patient refusal130401EG001

Harm

What it counts
Total, serious adverse events
Time frame
First subject first visit to end of trial within 7.25 years

Source ClinicalTrials.gov

Trial

Title
A Study of Avastin (Bevacizumab) Plus Crossover Fluoropyrimidine-Based Chemotherapy in Patients With Metastatic Colorectal Cancer.
NCT number
NCT00700102
Phases
PHASE3
Conditions
Colorectal Cancer
Interventions
Chemotherapy, Bevacizumab
Lead sponsor
Hoffmann-La Roche
Results first posted
2015-07-30

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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