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Comparison · NCT02429427-d2e50ba9

Celecoxib vs Placebo: Cardiovascular Mortality

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. Celecoxib vs Placebo: Cardiovascular Mortality. Trial comparisons, record NCT02429427-d2e50ba9. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02429427-d2e50ba9

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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 10.003420.001570.00744wilson
Risk in group 20.005760.002460.0134wilson
Risk difference, group 1 minus group 2-0.00234-0.01020.00286newcombe hybrid score
Risk ratio, group 1 over group 20.5940.1821.94log
Odds ratio, group 1 over group 20.5920.181.95log
Number needed to treat, for one fewer participant with the outcome on Celecoxib than on Placebo427from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Celecoxib
Patients in this arm will receive 400mg of celecoxib once daily. In addition, Hormone Receptor (+) patients will receive endocrine treatment according to local practice.~Celecoxib: Patients will receive 400mg of Celecoxib once daily for two years or until disease progression (if before the two years limit) or until development of unacceptable toxicities. In addition ER(+) patients will receive endocrine treatment according to local practice.
61,755OG000
Group 2Placebo
Patients in this arm will receive 2 tablets once daily. In addition Hormone Receptor (+) patients will receive endocrine treatment according to local practice.~Placebo: Two capsules once daily with food
5868OG001

Outcome

Type
SECONDARY
Title
Cardiovascular Mortality
Description
Number of deaths recorded as having cardiovascular involvement are reported by treatment group.
Time frame
Patients are followed up to 10 years, any deaths within this timeframe with cardiovascular involvement reported are included in the analysis.
Population
Safety population: This population includes all patients who start treatment, patients will be analysed by the treatment they received regardless of the group they were allocated to.

Source ClinicalTrials.gov

Trial

Title
European Celecoxib Trial in Primary Breast Cancer
NCT number
NCT02429427
Phases
PHASE3
Conditions
Breast Cancer
Interventions
Celecoxib, Placebo
Lead sponsor
Imperial College London
Results first posted
2020-06-23

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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