Comparison · NCT00053898-sae
Group 1: Tamoxifen + Anastrozole Placebo vs Group 2: Anastrazole + Tamoxifen Placebo: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Group 1: Tamoxifen + Anastrozole Placebo vs Group 2: Anastrazole + Tamoxifen Placebo: serious adverse events. Trial comparisons, record NCT00053898-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00053898-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0476 | 0.038 | 0.0594 | wilson | |
| Risk in group 2 | 0.0404 | 0.0316 | 0.0514 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00717 | -0.00745 | 0.0219 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.18 | 0.846 | 1.64 | log | |
| Odds ratio, group 1 over group 2 | 1.19 | 0.839 | 1.68 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Group 1: Tamoxifen + Anastrozole Placebo than on Group 2: Anastrazole + Tamoxifen Placebo | 140 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Group 1: Tamoxifen + Anastrozole Placebo | tamoxifen 20 mg/day and an anastrozole look-alike placebo for 5 years~Drug: tamoxifen citrate~20 mg/day and placebo for 5 years~Radiation: Radiation Therapy~Adjuvant radiation therapy | 73 | 1,535 | EG000 |
| Group 2 | Group 2: Anastrazole + Tamoxifen Placebo | anastrozole, 1 mg/day and a tamoxifen look-alike placebo for 5 years~Drug: anastrozole~1 mg/day and placebo for 5 years~Radiation: Radiation Therapy~Adjuvant radiation therapy | 62 | 1,535 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Source ClinicalTrials.gov
Trial
- Title
- Anastrozole or Tamoxifen in Treating Postmenopausal Women With Ductal Carcinoma in Situ Who Are Undergoing Lumpectomy and Radiation Therapy
- NCT number
- NCT00053898
- Phases
- PHASE3
- Conditions
- Breast Cancer
- Interventions
- anastrozole, tamoxifen citrate, Radiation Therapy
- Lead sponsor
- NSABP Foundation Inc
- Results first posted
- 2018-03-12
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00053898?tab=results
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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