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Comparison · NCT00617084-sae

1. Resolute - 12-13 Months vs 2. XIENCE V - 12-13 Months: serious adverse events

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. 1. Resolute - 12-13 Months vs 2. XIENCE V - 12-13 Months: serious adverse events. Trial comparisons, record NCT00617084-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00617084-sae

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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 10.3820.3540.41wilson
Risk in group 20.3750.3480.403wilson
Risk difference, group 1 minus group 20.00658-0.03310.0462newcombe hybrid score
Risk ratio, group 1 over group 21.020.9161.13log
Odds ratio, group 1 over group 21.030.8691.22log
Number needed to harm, for one more participant with a serious adverse event on 1. Resolute - 12-13 Months than on 2. XIENCE V - 12-13 Months152from 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 11. Resolute - 12-13 MonthsMedtronic Resolute - 12-13 Months4351,140EG000
Group 22. XIENCE V - 12-13 MonthsAbbott Xience V - 12-13 Months4321,152EG001

Harm

What it counts
Total, serious adverse events
Time frame
12 months

Source ClinicalTrials.gov

Trial

Title
Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent With Abbot Xience-V Stent
NCT number
NCT00617084
Phases
PHASE4
Conditions
Coronary Artery Disease
Interventions
Medtronic Endeavor Resolute, Abbott Xience V
Lead sponsor
Medtronic Vascular
Results first posted
2011-05-17

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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