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Comparison · NCT01205776-dd3f7a63

Percutaneous Coronary Intervention (PCI) vs Coronary Artery Bypass Graft (CABG): Number of Participants With Requirement for Blood Product Transfusion

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. Percutaneous Coronary Intervention (PCI) vs Coronary Artery Bypass Graft (CABG): Number of Participants With Requirement for Blood Product Transfusion. Trial comparisons, record NCT01205776-dd3f7a63. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01205776-dd3f7a63

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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 10.03160.02230.0448wilson
Risk in group 20.1250.1060.148wilson
Risk difference, group 1 minus group 2-0.0937-0.118-0.0702newcombe hybrid score
Risk ratio, group 1 over group 20.2520.1710.373log
Odds ratio, group 1 over group 20.2280.1510.344log
Number needed to treat, for one fewer participant with the outcome on Percutaneous Coronary Intervention (PCI) than on Coronary Artery Bypass Graft (CABG)10.78.4714.2from 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 1Percutaneous Coronary Intervention (PCI)Those patients receiving the XIENCE PRIME™ EECSS or XIENCE V® EECSS or XIENCE Xpedition™ EECSS or XIENCE PRO EECSS30948OG000
Group 2Coronary Artery Bypass Graft (CABG)Those patients receiving Coronary Artery Bypass Graft (CABG)120957OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Requirement for Blood Product Transfusion
Description
All TIMI definitions take into account blood transfusions, so that hemoglobin and hematocrit values are adjusted by 1 g/dl or 3%, respectively, for each unit of blood transfused. Therefore, the true change in hemoglobin or hematocrit if there has been an intervening transfusion between two blood measurements is calculated as follows:~* Δ Hemoglobin = \[baseline Hgb - post-transfusion Hgb\] + \[number of transfused units\];~* Δ Hematocrit = \[baseline Hct - post-transfusion Hct\] + \[number of transfused units X 3\].
Time frame
30 days
Population
ITT population. Analysis population includes subjects who had follow-up data at that time period.

Source ClinicalTrials.gov

Trial

Title
EXCEL Clinical Trial
NCT number
NCT01205776
Phases
NA
Conditions
Chronic Coronary Occlusion, Unprotected Left Main Coronary Artery Disease, Stent Thrombosis, Vascular Disease, Myocardial Ischemia, Coronary Artery Stenosis, Coronary Disease, Coronary Artery Disease, Coronary Restenosis
Interventions
Percutaneous Coronary Intervention, CABG
Lead sponsor
Abbott Medical Devices
Results first posted
2018-03-29

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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