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Comparison · NCT00754845-deaths

Arm I vs Arm II: deaths from any cause

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. Arm I vs Arm II: deaths from any cause. Trial comparisons, record NCT00754845-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00754845-deaths

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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 10.1040.08650.125wilson
Risk in group 20.1050.08690.126wilson
Risk difference, group 1 minus group 2-0.000547-0.02810.027newcombe hybrid score
Risk ratio, group 1 over group 20.9950.7651.29log
Odds ratio, group 1 over group 20.9940.7421.33log
Number needed to treat, for one fewer death from any cause on Arm I than on Arm II1,830from 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 1Arm IPatients receive oral letrozole once daily for up to 5 years in the absence of unacceptable toxicity, disease recurrence, or development of a second malignancy.~letrozole: Given orally100959EG000
Group 2Arm IIPatients receive oral placebo once daily for up to 5 years in the absence of unacceptable toxicity, disease recurrence, or development of a second malignancy.~placebo: Given orally100954EG001

Harm

What it counts
Total, all-cause mortality
Time frame
During protocol treatment of 5 years

Source ClinicalTrials.gov

Trial

Title
Letrozole in Breast Cancer Who Have Received 5 Years of Aromatase Inhibitor Therapy
NCT number
NCT00754845
Phases
PHASE3
Conditions
Breast Cancer
Interventions
letrozole, placebo
Lead sponsor
Canadian Cancer Trials Group
Results first posted
2018-11-19

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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