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Trial · NCT00053898

Results by group20

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Percentage of Patients Free From Breast CancerGroup 1: Tamoxifen + Anastrozole Placebo89.1percentage of participants event-free
Percentage of Patients Free From Breast CancerGroup 2: Anastrozole + Tamoxifen Placebo93.1percentage of participants event-free
Percentage of Patients Free From Invasive Breast CancerGroup 1: Tamoxifen + Anastrozole Placebo93.3percentage of participants event-free
Percentage of Patients Free From Invasive Breast CancerGroup 2: Anastrozole + Tamoxifen Placebo96.4percentage of participants event-free
Percentage of Patients Free From Ipsilateral RecurrenceGroup 1: Tamoxifen + Anastrozole Placebo94.6percentage of participants event-free
Percentage of Patients Free From Ipsilateral RecurrenceGroup 2: Anastrozole + Tamoxifen Placebo96.4percentage of participants event-free
Percentage of Patients Free From Contralateral Breast CancerGroup 1: Tamoxifen + Anastrozole Placebo94.7percentage of participants event-free
Percentage of Patients Free From Contralateral Breast CancerGroup 2: Anastrozole + Tamoxifen Placebo97.0percentage of participants event-free
Percentage of Patients Free From Non-breast Secondary CancerGroup 1: Tamoxifen + Anastrozole Placebo91.5percentage of participants event-free
Percentage of Patients Free From Non-breast Secondary CancerGroup 2: Anastrozole + Tamoxifen Placebo91.9percentage of participants event-free
Percentage of Patients Free From Osteoporotic FracturesGroup 1: Tamoxifen + Anastrozole Placebo96.0percentage of participants event-free
Percentage of Patients Free From Osteoporotic FracturesGroup 2: Anastrozole + Tamoxifen Placebo95.3percentage of participants event-free
Percentage of Patients Alive and Disease-freeGroup 1: Tamoxifen + Anastrozole Placebo77.9percentage of participants event-free
Percentage of Patients Alive and Disease-freeGroup 2: Anastrozole + Tamoxifen Placebo82.7percentage of participants event-free
Percentage of Patients Alive (Overall Survival)Group 1: Tamoxifen + Anastrozole Placebo92.1percentage of participants event-free
Percentage of Patients Alive (Overall Survival)Group 2: Anastrozole + Tamoxifen Placebo92.5percentage of participants event-free
Quality of Life-Short Form 12 (SF-12) Physical Health Component ScoreGroup 1: Tamoxifen + Anastrozole Placebo46.20Standard Deviation 10.13units on a scale
Quality of Life-Short Form 12 (SF-12) Physical Health Component ScoreGroup 2: Anastrozole + Tamoxifen Placebo45.38Standard Deviation 10.25units on a scale
Quality-adjusted Survival TimeGroup 1: Tamoxifen + Anastrozole Placebo104.495% Confidence Interval 101.8 to 106.9months
Quality-adjusted Survival TimeGroup 2: Anastrozole + Tamoxifen Placebo102.995% Confidence Interval 100.9 to 104.9months

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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