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Comparison · NCT00003830-325f713c

Arm I:Sentinel Node Resection+Conventional Axillary Dissection vs Arm II: Sentinel Node Resection Followed by Node Examination: Morbidity - Number of Participants With Residual Arm Numbness

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:Sentinel Node Resection+Conventional Axillary Dissection vs Arm II: Sentinel Node Resection Followed by Node Examination: Morbidity - Number of Participants With Residual Arm Numbness. Trial comparisons, record NCT00003830-325f713c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00003830-325f713c

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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 10.3050.2810.331wilson
Risk in group 20.07510.06230.0903wilson
Risk difference, group 1 minus group 20.230.2020.259newcombe hybrid score
Risk ratio, group 1 over group 24.063.324.98log
Odds ratio, group 1 over group 25.414.296.83log
Number needed to treat, for one more participant with the outcome on Arm I:Sentinel Node Resection+Conventional Axillary Dissection than on Arm II: Sentinel Node Resection Followed by Node Examination4.343.874.96from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Arm I:Sentinel Node Resection+Conventional Axillary DissectionSentinel node resection immediately followed by axillary dissection~conventional surgery: Sentinel node resection immediately followed by axillary dissection.4081,336OG000
Group 2Arm II: Sentinel Node Resection Followed by Node Examination
Sentinel node resection followed by node examination then axillary dissection if positive sentinel node.~Sentinel node resection followed by node examination: Sentinel node resection followed by node examination then axillary dissection if positive sentinel node. No axillary dissection for negative sentinel node.
1031,371OG001

Outcome

Type
PRIMARY
Title
Morbidity - Number of Participants With Residual Arm Numbness
Description
Morbidity as measured by residual arm numbness
Time frame
before and after surgery (within 30 days of randomization)
Population
Data missing or unknown for some patients

Source ClinicalTrials.gov

Trial

Title
Surgery to Remove Sentinel Lymph Nodes With or Without Removing Lymph Nodes in the Armpit in Treating Women With Breast Cancer
NCT number
NCT00003830
Phases
PHASE3
Conditions
Breast Cancer
Interventions
conventional surgery, Sentinel node resection followed by node examination
Lead sponsor
NSABP Foundation Inc
Results first posted
2017-12-13

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.govNone 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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