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Comparison · NCT00083174-7a8aa8e9

Randomization Period: Exemestane vs Randomization Period: Placebo: Incidence of All Clinical Fractures

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. Randomization Period: Exemestane vs Randomization Period: Placebo: Incidence of All Clinical Fractures. Trial comparisons, record NCT00083174-7a8aa8e9. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00083174-7a8aa8e9

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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 10.06650.05690.0776wilson
Risk in group 20.06360.05420.0745wilson
Risk difference, group 1 minus group 20.00291-0.01160.0174newcombe hybrid score
Risk ratio, group 1 over group 21.050.8381.31log
Odds ratio, group 1 over group 21.050.8271.33log
Number needed to treat, for one more participant with the outcome on Randomization Period: Exemestane than on Randomization Period: Placebo344from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Randomization Period: Exemestaneone 25 mg tablet daily in am1492,240OG000
Group 2Randomization Period: Placeboone tablet daily in am1432,248OG001

Outcome

Type
SECONDARY
Title
Incidence of All Clinical Fractures
Description
Time frame
During protocol treatment over randomization period of study (up to 5 years)
Population
Women who have received treatment

Source ClinicalTrials.gov

Trial

Title
Exemestane in Preventing Cancer in Postmenopausal Women at Increased Risk of Developing Breast Cancer
NCT number
NCT00083174
Phases
PHASE3
Conditions
Breast Cancer
Interventions
exemestane
Lead sponsor
NCIC Clinical Trials Group
Results first posted
2013-05-20

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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