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Comparison · NCT00023595-b5f2bc28

H01: Medication vs Total H01: Medication + CABG: H01: Cardiac Procedure: Implantable Cardioverter Defibrillator (ICD)

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. H01: Medication vs Total H01: Medication + CABG: H01: Cardiac Procedure: Implantable Cardioverter Defibrillator (ICD). Trial comparisons, record NCT00023595-b5f2bc28. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00023595-b5f2bc28

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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 10.1630.1350.194wilson
Risk in group 20.1250.1010.153wilson
Risk difference, group 1 minus group 20.0382-0.001350.0778newcombe hybrid score
Risk ratio, group 1 over group 21.310.991.72log
Odds ratio, group 1 over group 21.370.9891.89log
Number needed to treat, for one more participant with the outcome on H01: Medication than on Total H01: Medication + CABG26.2from 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 1H01: Medication
H01 patients were randomized to medical therapy alone. Throughout the trial follow-up period, the use of guideline-recommended medications and devices for the treatment of heart failure and CAD was strongly emphasized for all patients in this treatment arm.
98602OG000
Group 2Total H01: Medication + CABG
H01 patients were randomized to medical therapy plus CABG. In addition to the guideline-recommended medications, coronary artery bypass graft (CABG) surgery was to be performed for patients randomized to this treatment arm.~The Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.
76610OG001

Outcome

Type
SECONDARY
Title
H01: Cardiac Procedure: Implantable Cardioverter Defibrillator (ICD)
Description
Time frame
5 years post randomization
Population
The Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.

Source ClinicalTrials.gov

Trial

Title
Comparison of Surgical and Medical Treatment for Congestive Heart Failure and Coronary Artery Disease
NCT number
NCT00023595
Phases
PHASE3
Conditions
Cardiovascular Diseases, Coronary Disease, Heart Failure, Congestive, Heart Diseases
Interventions
CABG surgery plus MED, Active Medication Alone, CABG plus MED and SVR
Lead sponsor
Duke University
Results first posted
2017-07-24

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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