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Trial ยท NCT00023595

Comparison of Surgical and Medical Treatment for Congestive Heart Failure and Coronary Artery Disease

NCT00023595, Phase 3, Completed, Duke University; results first posted 2017-07-24

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Comparison of Surgical and Medical Treatment for Congestive Heart Failure and Coronary Artery Disease. Trials, record NCT00023595. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00023595

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Comparison of Surgical and Medical Treatment for Congestive Heart Failure and Coronary Artery Disease
NCT number
NCT00023595
Status
Completed
Phases
Phase 3
Enrollment
2,136 participants, actual
Lead sponsor
Duke University
Conditions
Cardiovascular Diseases, Coronary Disease, Heart Failure, Congestive, Heart Diseases
Interventions
CABG surgery plus MED, Active Medication Alone, CABG plus MED and SVR
First posted
2001-09-11
Last updated
2019-09-19
Results first posted
2017-07-24

Source ClinicalTrials.gov

Registered outcomes101

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryH01: All Cause Mortality5 years post randomization
PrimaryH01: All Cause Mortality10 years post randomization
PrimaryH02: All-cause Mortality or Cardiovascular Hospitalization5 years post randomization
SecondaryH01: Cardiovascular Mortality (Defined as Sudden Death or Death Attributed to Recurrent MI, HF, a Cardiovascular Procedure, Stroke, or Other Cardiovascular Etiology).10 years post randomization
SecondaryH01: Cardiovascular Mortality (Defined as Sudden Death or Death Attributed to Recurrent MI, HF, a Cardiovascular Procedure, Stroke, or Other Cardiovascular Etiology).5 years post randomization
SecondaryH01: Mortality or Cardiovascular Hospitalizationup to 5 years post randomization
SecondaryH01: Mortality or Cardiovascular Hospitalizationup to 10 years post randomization
SecondaryH02: All-cause Mortalityup to 5 years
SecondaryH01: All-cause Mortality Within 30 Days After Randomization30 days post randomization
SecondaryH02: All-cause Mortality Within 30 Days After Randomization30 days post randomization

Outcomes101

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYH01: All Cause Mortality5 years post randomizationThe Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
PRIMARYH01: All Cause Mortality10 years post randomizationThe Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
PRIMARYH02: All-cause Mortality or Cardiovascular Hospitalization5 years post randomizationThe Total H02: Medication + CABG group includes the H02: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
SECONDARYH01: Cardiovascular Mortality (Defined as Sudden Death or Death Attributed to Recurrent MI, HF, a Cardiovascular Procedure, Stroke, or Other Cardiovascular Etiology).10 years post randomizationThe Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
SECONDARYH01: Cardiovascular Mortality (Defined as Sudden Death or Death Attributed to Recurrent MI, HF, a Cardiovascular Procedure, Stroke, or Other Cardiovascular Etiology).5 years post randomizationThe Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
SECONDARYH01: Mortality or Cardiovascular Hospitalizationup to 5 years post randomizationThe Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
SECONDARYH01: Mortality or Cardiovascular Hospitalizationup to 10 years post randomizationThe Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
SECONDARYH02: All-cause Mortalityup to 5 yearsThe Total H02: Medication + CABG group includes the H02: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
SECONDARYH01: All-cause Mortality Within 30 Days After Randomization30 days post randomizationThe Total H01: Medication + CABG group includes the H01: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG arm.participantsNUMBER
SECONDARYH02: All-cause Mortality Within 30 Days After Randomization30 days post randomizationThe Total H02: Medication + CABG group includes the H02: Medication + CABG group and those 76 patients who belong to H01+H02: Medication + CABG armparticipantsNUMBER

Results by group690

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
H01: All Cause MortalityH01: Medication244participants
H01: All Cause MortalityTotal H01: Medication + CABG218participants
H01: All Cause MortalityH01: Medication398participants
H01: All Cause MortalityTotal H01: Medication + CABG359participants
H02: All-cause Mortality or Cardiovascular HospitalizationH02: Medication+CABG+SVR289participants
H02: All-cause Mortality or Cardiovascular HospitalizationTotal H02: Medication+CABG292participants
H01: Cardiovascular Mortality (Defined as Sudden Death or Death Attributed to Recurrent MI, HF, a Cardiovascular Procedure, Stroke, or Other Cardiovascular Etiology).Total H01: Medication + CABG247participants
H01: Cardiovascular Mortality (Defined as Sudden Death or Death Attributed to Recurrent MI, HF, a Cardiovascular Procedure, Stroke, or Other Cardiovascular Etiology).H01: Medication297participants
H01: Cardiovascular Mortality (Defined as Sudden Death or Death Attributed to Recurrent MI, HF, a Cardiovascular Procedure, Stroke, or Other Cardiovascular Etiology).Total H01: Medication + CABG168participants
H01: Cardiovascular Mortality (Defined as Sudden Death or Death Attributed to Recurrent MI, HF, a Cardiovascular Procedure, Stroke, or Other Cardiovascular Etiology).H01: Medication201participants

Participant flow30

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
5 Year Follow upSTARTEDH01: Medication602
5 Year Follow upSTARTEDH01: Medication + CABG534
5 Year Follow upSTARTEDH01+H02: Medication + CABG76
5 Year Follow upSTARTEDH02: Medication+CABG423
5 Year Follow upSTARTEDH02: Medication+CABG+SVR501
5 Year Follow upCOMPLETEDH01: Medication600
5 Year Follow upCOMPLETEDH01: Medication + CABG532
5 Year Follow upCOMPLETEDH01+H02: Medication + CABG75
5 Year Follow upCOMPLETEDH02: Medication+CABG416
5 Year Follow upCOMPLETEDH02: Medication+CABG+SVR498

Adverse events710

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousABSCESSInfections and infestationsH01: Medication0602
seriousABSCESSInfections and infestationsH01: Medication + CABG0534
seriousABSCESSInfections and infestationsH01 & H02: Medication+CABG076
seriousABSCESSInfections and infestationsH02: Medication+CABG0423
seriousABSCESSInfections and infestationsH02: Medication+CABG+SVR1501
seriousACUTE CORONARY SYNDROMECardiac disordersH01: Medication1602
seriousACUTE CORONARY SYNDROMECardiac disordersH01: Medication + CABG0534
seriousACUTE CORONARY SYNDROMECardiac disordersH01 & H02: Medication+CABG076
seriousACUTE CORONARY SYNDROMECardiac disordersH02: Medication+CABG0423
seriousACUTE CORONARY SYNDROMECardiac disordersH02: Medication+CABG+SVR0501

Adverse event totals15

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityH01: Medication
Total, all-cause mortalityH01: Medication + CABG
Total, all-cause mortalityH01 & H02: Medication+CABG
Total, all-cause mortalityH02: Medication+CABG
Total, all-cause mortalityH02: Medication+CABG+SVR
Total, other adverse eventsH01: Medication00
Total, other adverse eventsH01: Medication + CABG00
Total, other adverse eventsH01 & H02: Medication+CABG00
Total, other adverse eventsH02: Medication+CABG00
Total, other adverse eventsH02: Medication+CABG+SVR00

Papers36

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
18023680BACKGROUNDPubMed
19329820DERIVEDPubMed
19376309DERIVEDPubMed
20670760DERIVEDPubMed
20670761DERIVEDPubMed
21463150DERIVEDPubMed
21463153DERIVEDPubMed
22553307DERIVEDPubMed
22584648DERIVEDPubMed
23500234DERIVEDPubMed

1 to 10 of 36

See all 36 papers

Grants8

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource
R01HL105853STICHESAL-KHALIDI, HUSSEINDUKE UNIVERSITYNATIONAL HEART, LUNG, AND BLOOD INSTITUTE2011 to 2015NIH RePORTER
U01HL069015STICH Trial-Coordinating CenterJONES, ROBERT HDUKE UNIVERSITYNATIONAL HEART, LUNG, AND BLOOD INSTITUTE2002 to 2011NIH RePORTER
U01HL069013STICH Trial-Statistical and Data Coordinatiing CenterLEE, KERRY LDUKE UNIVERSITYNATIONAL HEART, LUNG, AND BLOOD INSTITUTE2002 to 2010NIH RePORTER
U01HL069011STICH TRIAL- Economics & Quality of Life Core LaboratoryMARK, DANIEL BDUKE UNIVERSITYNATIONAL HEART, LUNG, AND BLOOD INSTITUTE2002 to 2008NIH RePORTER
U01HL069009STICH TRIAL - NEUROHORMONAL/ CYTOKINE/ GENETIC CORE LABFELDMAN, ARTHUR MTHOMAS JEFFERSON UNIVERSITYNATIONAL HEART, LUNG, AND BLOOD INSTITUTE2002 to 2007NIH RePORTER
U01HL069010STICH Trial-Echocardiographic Core LaboratoryOH, JAE KMAYO CLINIC ROCHESTERNATIONAL HEART, LUNG, AND BLOOD INSTITUTE2002 to 2007NIH RePORTER
U01HL069012STICH Trial Radionuclide Core LaboratoryBONOW, ROBERT ONORTHWESTERN UNIVERSITY AT CHICAGONATIONAL HEART, LUNG, AND BLOOD INSTITUTE2002 to 2007NIH RePORTER
U01HL072683STICH-Trial Cardiovascular Magenetic Resonance Core LabPOHOST, GERALD MICHAELUNIVERSITY OF SOUTHERN CALIFORNIANATIONAL HEART, LUNG, AND BLOOD INSTITUTE2002 to 2007NIH RePORTER

Trial comparisons37

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
H01: Medication vs Total H01: Medication + CABG: H01: All Cause MortalityTrial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: All-cause Mortality Within 30 Days After RandomizationTrial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: Mortality or Cardiovascular HospitalizationTrial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: All-cause (Unplanned and Elective) HospitalizationTrial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: StrokeTrial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: All-cause Mortality or Revascularization (CABG or PCI)Trial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: Cardiac Procedure: Implantable Cardioverter Defibrillator (ICD)Trial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: All-cause Mortality, Heart Transplant or LVADTrial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: Mortality or Cardiovascular HospitalizationTrial comparisons
H01: Medication vs Total H01: Medication + CABG: H01: StrokeTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00023595

GET https://conductscience.org/api/trials/v1/NCT00023595/registered?page=2