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Trial · NCT02270242

Ticagrelor With Aspirin or Alone in High-Risk Patients After Coronary Intervention

NCT02270242, Phase 4, Completed, Icahn School of Medicine at Mount Sinai; results first posted 2020-08-19

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Ticagrelor With Aspirin or Alone in High-Risk Patients After Coronary Intervention. Trials, record NCT02270242. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02270242

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Trial

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

Title
Ticagrelor With Aspirin or Alone in High-Risk Patients After Coronary Intervention
NCT number
NCT02270242
Status
Completed
Phases
Phase 4
Enrollment
9,006 participants, actual
Lead sponsor
Icahn School of Medicine at Mount Sinai
Conditions
Cardiovascular Disease, Interventional Cardiology
Interventions
Aspirin, Placebo, ticagrelor
First posted
2014-10-21
Last updated
2021-01-13
Results first posted
2020-08-19
Limitations and caveats
Limitations include lack of power to detect differences in the risk of important yet rare clinical events, e.g stent thrombosis and stroke; and trial may not be generalizable to all patients undergoing PCI due to high risk criteria.

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants With BARC Type 2, 3, or 512 months after randomization
Number of participants with first occurrence of clinically relevant bleeding episode, defined as Bleeding Academic Research Consortium (BARC) Types 2, 3 or 5 bleeding. BARC bleeding types range from 0 (no bleeding) to 5 (fatal bleeding).
SecondaryNumber of Participants With Ischemic Episode12 months after randomizationNumber of participants with first occurrence of confirmed all-cause death, non-fatal myocardial infarction or stroke.

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants With BARC Type 2, 3, or 512 months after randomizationData for the intention-to-treat populationParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants With Ischemic Episode12 months after randomizationdata for the per-protocol population , i.e., the participants who underwent randomization and had no major deviations from the protocol.ParticipantsCOUNT_OF_PARTICIPANTS

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With BARC Type 2, 3, or 5Placebo + Ticagrelor141Participants
Number of Participants With BARC Type 2, 3, or 5Aspirin + Ticagrelor250Participants
Number of Participants With Ischemic EpisodePlacebo + Ticagrelor135Participants
Number of Participants With Ischemic EpisodeAspirin + Ticagrelor137Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPlacebo + Ticagrelor3,555
Overall StudySTARTEDAspirin + Ticagrelor3,564
Overall StudyCOMPLETEDPlacebo + Ticagrelor3,496
Overall StudyCOMPLETEDAspirin + Ticagrelor3,511
Overall StudyNOT COMPLETEDPlacebo + Ticagrelor59
Overall StudyNOT COMPLETEDAspirin + Ticagrelor53

Adverse events8

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

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousMyocardial InfarctionCardiac disordersPlacebo + Ticagrelor953,524
seriousMyocardial InfarctionCardiac disordersAspirin + Ticagrelor973,515
seriousIschemic StrokeVascular disordersPlacebo + Ticagrelor183,524
seriousIschemic StrokeVascular disordersAspirin + Ticagrelor103,515
seriousStent Thrombosis, definite or probableInjury, poisoning and procedural complicationsPlacebo + Ticagrelor143,524
seriousStent Thrombosis, definite or probableInjury, poisoning and procedural complicationsAspirin + Ticagrelor203,515
seriousBARC 235Vascular disordersPlacebo + Ticagrelor1413,555
seriousBARC 235Vascular disordersAspirin + Ticagrelor2503,564

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo + Ticagrelor343,524
Total, all-cause mortalityAspirin + Ticagrelor453,515
Total, other adverse eventsPlacebo + Ticagrelor03,555
Total, other adverse eventsAspirin + Ticagrelor03,564
Total, serious adverse eventsPlacebo + Ticagrelor2623,555
Total, serious adverse eventsAspirin + Ticagrelor3703,564

Papers38

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
15289388BACKGROUNDPubMed
15852223BACKGROUNDPubMed
16476694BACKGROUNDPubMed
16621870BACKGROUNDPubMed
16996826BACKGROUNDPubMed
17084243BACKGROUNDPubMed
17470709BACKGROUNDPubMed
17679616BACKGROUNDPubMed
17980251BACKGROUNDPubMed
17982182BACKGROUNDPubMed

1 to 10 of 38

See all 38 papers

Grants0

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.

None in this release.

Trial comparisons4

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

ComparisonSource
Placebo + Ticagrelor vs Aspirin + Ticagrelor: Number of Participants With Ischemic EpisodeTrial comparisons
Placebo + Ticagrelor vs Aspirin + Ticagrelor: Number of Participants With BARC Type 2, 3, or 5Trial comparisons
Placebo + Ticagrelor vs Aspirin + Ticagrelor: deaths from any causeTrial comparisons
Placebo + Ticagrelor vs Aspirin + Ticagrelor: 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.

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/NCT02270242

GET https://conductscience.org/api/trials/v1/NCT02270242/papers?page=2