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NCT05997693RecruitingPhase 3

One-Month DAPT in CABG Patients

One Month Dual Antiplatelet Therapy With Ticagrelor in Coronary Artery Bypass Graft Patients

Source: ClinicalTrials.gov · Last updated 22 Dec 2025

Brief summary (registry, in English)

The purpose of this study is to compare the effect of ticagrelor plus low-dose aspirin versus low-dose aspirin alone in patients with chronic coronary disease undergoing coronary artery bypass grafting.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
700 (estimated)
First submitted
26 Jul 2023
Start date
15 Aug 2024
Primary completion date
31 Jan 2027
Lead sponsor
Weill Medical College of Cornell University
NCT number
NCT05997693
EU CT number
2023-506613-22-00
EudraCT number
2023-506613-22

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 700
  • From 15 Aug 2024 to the primary completion date, 31 Jan 2027
  • 23 sites in 6 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any indication for dual antiplatelet therapy, including
    • Acute/recent (within 1 year) ACS (NSTE-ACS or STEMI)
    • Recent PCI requiring continuation of dual antiplatelet therapy after CABG
  • Any concomitant cardiac or non-cardiac procedure;
  • Contraindications to the use of ticagrelor, including
    • Known hypersensitivity to ticagrelor
    • Active pathological bleeding (including, but not limited to gastrointestinal or intracranial bleeding)
    • History of intracranial hemorrhage
    • Concomitant therapy with strong CYP3A4 inhibitors (eg ketoconazole, clarithromycin, nefazodone, ritonavir, atazanavir)
  • Participating in another investigational device or drug study;

Other illness

  • Planned cardiac or non-cardiac surgery within one year;
  • Any major perioperative complication including, but not limited to, stroke, TIA, MI, CABG-related bleeding (BARC type 4), sepsis.

Age

  • Preoperative end-organ dysfunction (dialysis, moderate to severe liver failure, respiratory failure), cancer or other non-cardiac comorbidity with a life expectancy \<5 years;

Other

  • Current or anticipated use of oral anticoagulation;
  • Paroxysmal, persistent or permanent atrial fibrillation;
  • Inability to use the saphenous vein;
  • Contraindications to the use of aspirin;
  • Inability to undergo coronary computed tomographic angiography (CCTA);
  • Women of childbearing potential

Who the study is looking for

  • Age ≥18 years
  • Elective first-time CABG with use of ≥1 saphenous vein graft;
  • Ability to sign informed consent and comply with all study procedures, including follow-up for at least 5 years.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (23)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Medical University of Graz
Coordinator of this site? Confirm its status
GrazAustriaRecruiting
Medizinische Universitaet Innsbruck
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InnsbruckAustriaRecruiting
Johannes Kepler University
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LinzAustriaRecruiting
Noe LGA Gesundheit Region Mitte GmbH
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St. PoeltenAustriaRecruiting
Medical University of Vienna
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ViennaAustriaRecruiting
University of Ottawa Heart Institute
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OttawaCanadaNot yet recruiting
Center China Fuwai Hospital
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BeijingChinaRecruiting
Beijing Anzhen Hospital
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BeijingChinaRecruiting
Jilin Heart Hospital
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ChangchunChinaRecruiting
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
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ShanghaiChinaRecruiting
Universitaetsklinikum Duesseldorf AöR
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DuesseldorfGermanyRecruiting
Universitaetsklinikum Essen (AoR)
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EssenGermanyRecruiting
Medical Center- University of Freiburg
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Freiburg im BreisgauGermanyRecruiting
Justus-Liebig-Universitaet Giessen
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GiessenGermanyRecruiting
Universitaetsklinikum Jena KöR
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JenaGermanyRecruiting
TUM Klinikum Deutsches Herzzentrum
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MunichGermanyRecruiting
Robert Bosch Gesellschaft fuer medizinische Forschung mbH
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StuttgartGermanyRecruiting
Universitaetsklinikum Wuerzburg AöR
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WuerzburgGermanyRecruiting
Sahlgrenska University Hospital-Vastra Gotalandsregionen
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GoteborgSwedenRecruiting
Region Skane Skanes Universitetssjukhus
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LundSwedenRecruiting
Englewood Hospital
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EnglewoodUnited StatesRecruiting
NewYork-Presbyterian: Queens Hospital
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FlushingUnited StatesRecruiting
Weill Cornell Medicine
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New YorkUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.