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Trial ยท NCT01471522

International Study of Comparative Health Effectiveness With Medical and Invasive Approaches (ISCHEMIA)

NCT01471522, Not applicable, Completed, NYU Langone Health; results first posted 2020-07-23

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. International Study of Comparative Health Effectiveness With Medical and Invasive Approaches (ISCHEMIA). Trials, record NCT01471522. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01471522

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Trial

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

Title
International Study of Comparative Health Effectiveness With Medical and Invasive Approaches (ISCHEMIA)
NCT number
NCT01471522
Status
Completed
Phases
Not applicable
Enrollment
5,179 participants, actual
Lead sponsor
NYU Langone Health
Conditions
Cardiovascular Diseases, Coronary Disease, Coronary Artery Disease, Heart Diseases, Myocardial Ischemia
Interventions
cardiac catheterization, coronary artery bypass graft surgery, percutaneous coronary intervention, Lifestyle, Medication
First posted
2011-11-15
Last updated
2023-06-01
Results first posted
2020-07-23

Source ClinicalTrials.gov

Registered outcomes12

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

ListOutcomeTime frameDescription
PrimaryPrimary Composite Outcome: Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest3.2 year follow-up (median)
PrimaryCumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)5 years
This measure represents the estimated cumulative probability of experiencing the primary endpoint within the indicated timeframe in each treatment group. The interpretation of the measure is similar to Kaplan-Meier event rates. Estimates are expressed as percentages ranging from 0% (endpoint is certain not to occur) to 100% (endpoint is certain to occur).
PrimaryNumber of Participants That Experienced Death From Cardiovascular Causes or Myocardial Infarction5 years
PrimaryCumulative Event Rate of Death From Cardiovascular Causes or Myocardial Infarction5 years
This measure represents the estimated cumulative probability of experiencing Death from cardiovascular causes or myocardial infarction within the indicated timeframe in each treatment group. The interpretation of the measure is similar to Kaplan-Meier event rates. Estimates are expressed as percentages ranging from 0% (endpoint is certain not to occur) to 100% (endpoint is certain to occur).
PrimaryNumber of Participants That Experienced Death From Any Cause5 years
PrimaryCumulative Event Rate of Death From Any Cause5 years
PrimaryNumber of Participants That Experienced Myocardial Infarction5 years
PrimaryCumulative Event Rate of Myocardial Infarction5 years
PrimaryEstimated Difference in Cumulative Event Rate ( %) of Primary Composite Outcome: Invasive Minus Conservative5 yearsThe primary composite outcome includes death from cardiovascular causes, myocardial infarction, or hospitalization for unstable angina, heart failure, or resuscitated cardiac arrest.
PrimaryEstimated Difference in Cumulative Event Rate of Death From Cardiovascular Causes: Invasive Minus Conservative or Myocardial Infarction Between Invasive and Conservative Strategies5 years

Outcomes12

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPrimary Composite Outcome: Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest3.2 year follow-up (median)ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYCumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)5 yearscumulative event rate - %NUMBER
PRIMARYNumber of Participants That Experienced Death From Cardiovascular Causes or Myocardial Infarction5 yearsParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYCumulative Event Rate of Death From Cardiovascular Causes or Myocardial Infarction5 yearsCumulative event rate -- %NUMBER
PRIMARYNumber of Participants That Experienced Death From Any Cause5 yearsParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYCumulative Event Rate of Death From Any Cause5 yearsCumulative event rate -- %NUMBER
PRIMARYNumber of Participants That Experienced Myocardial Infarction5 yearsParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYCumulative Event Rate of Myocardial Infarction5 yearsCumulative event rate -- %NUMBER
PRIMARYEstimated Difference in Cumulative Event Rate ( %) of Primary Composite Outcome: Invasive Minus Conservative5 yearsInvasive = 2588; Conservative = 2591cumulative event rate - %NUMBER
PRIMARYEstimated Difference in Cumulative Event Rate of Death From Cardiovascular Causes: Invasive Minus Conservative or Myocardial Infarction Between Invasive and Conservative Strategies5 yearsInvasive = 2588; Conservative = 2591cumulative event rate - %NUMBER

Results by group80

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

OutcomeGroupCategoryValueSpreadUnits
Primary Composite Outcome: Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac ArrestInvasive Strategy (INV)318Participants
Primary Composite Outcome: Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac ArrestConservative Strategy352Participants
Cumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)Invasive Strategy (INV)At 6 months5.3cumulative event rate - %
Cumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)Conservative StrategyAt 6 months3.4cumulative event rate - %
Cumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)Invasive Strategy (INV)At 1 year7.0cumulative event rate - %
Cumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)Conservative StrategyAt 1 year5.4cumulative event rate - %
Cumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)Invasive Strategy (INV)At 2 years9.0cumulative event rate - %
Cumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)Conservative StrategyAt 2 years9.5cumulative event rate - %
Cumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)Invasive Strategy (INV)At 3 years11.3cumulative event rate - %
Cumulative Event Rate of Primary Composite Outcome (Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest)Conservative StrategyAt 3 years12.7cumulative event rate - %

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDInvasive Strategy (INV)2,588
Overall StudySTARTEDConservative Strategy2,591
Overall StudyCOMPLETEDInvasive Strategy (INV)2,524
Overall StudyCOMPLETEDConservative Strategy2,543
Overall StudyNOT COMPLETEDInvasive Strategy (INV)64
Overall StudyNOT COMPLETEDConservative Strategy48

Adverse events14

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

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousCardiovascular DeathCardiac disordersInvasive Strategy (INV)922,58892
seriousCardiovascular DeathCardiac disordersConservative Strategy1112,591111
seriousProcedural Myocardial InfarctionCardiac disordersInvasive Strategy (INV)702,58870
seriousProcedural Myocardial InfarctionCardiac disordersConservative Strategy242,59124
seriousNon-procedural Myocardial InfarctionCardiac disordersInvasive Strategy (INV)1302,588130
seriousNon-procedural Myocardial InfarctionCardiac disordersConservative Strategy1962,591196
seriousHospitalization for Unstable AnginaCardiac disordersInvasive Strategy (INV)162,58816
seriousHospitalization for Unstable AnginaCardiac disordersConservative Strategy322,59132
seriousHospitalization for Heart FailureCardiac disordersInvasive Strategy (INV)512,58851
seriousHospitalization for Heart FailureCardiac disordersConservative Strategy252,59125

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityInvasive Strategy (INV)1452,588
Total, all-cause mortalityConservative Strategy1442,591
Total, other adverse eventsInvasive Strategy (INV)02,588
Total, other adverse eventsConservative Strategy02,591
Total, serious adverse eventsInvasive Strategy (INV)3182,588
Total, serious adverse eventsConservative Strategy3522,591

Papers53

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
22137077BACKGROUNDPubMed
23963599BACKGROUNDPubMed
26373291DERIVEDPubMed
26616030DERIVEDPubMed
26683627DERIVEDPubMed
27326241DERIVEDPubMed
29778671BACKGROUNDPubMed
30810700BACKGROUNDPubMed
30994826DERIVEDPubMed
32227128DERIVEDPubMed

1 to 10 of 53

See all 53 papers

Grants1

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 years
U01HL105907The Ischemia Trial - CCCHOCHMAN, JUDITH SNEW YORK UNIVERSITY SCHOOL OF MEDICINENATIONAL HEART, LUNG, AND BLOOD INSTITUTE2011 to 2019

Trial comparisons6

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

ComparisonSource
Invasive Strategy (INV) vs Conservative Strategy: Number of Participants That Experienced Death From Any CauseTrial comparisons
Invasive Strategy (INV) vs Conservative Strategy: Number of Participants That Experienced Death From Cardiovascular Causes or Myocardial InfarctionTrial comparisons
Invasive Strategy (INV) vs Conservative Strategy: Number of Participants That Experienced Myocardial InfarctionTrial comparisons
Invasive Strategy (INV) vs Conservative Strategy: Primary Composite Outcome: Death From Cardiovascular Causes, Myocardial Infarction, or Hospitalization for Unstable Angina, Heart Failure, or Resuscitated Cardiac Arrest
Trial comparisons
Invasive Strategy (INV) vs Conservative Strategy: deaths from any causeTrial comparisons
Invasive Strategy (INV) vs Conservative Strategy: serious adverse eventsTrial 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.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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/NCT01471522

GET https://conductscience.org/api/trials/v1/NCT01471522/results?page=2