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NCT03560310Active, not recruitingPhase 4

Ticagrelor and ASA vs. ASA Only After Isolated Coronary Artery Bypass Grafting in Patients With Acute Coronary Syndrome

Dual Antiplatelet Therapy With Ticagrelor and Acetylsalicylic Acid (ASA) vs. ASA Only After Isolated Coronary Artery Bypass Grafting in Patient With Acute Coronary Syndrome

Source: ClinicalTrials.gov · Last updated 2 Sept 2025

Brief summary (registry, in English)

The study is a Randomised Registry-based Clinical Trial (RRCT) to assess whether dual antiplatelet therapy with ticagrelor and ASA compared to ASA alone improves outcome after isolated CABG in patients with acute coronary syndrome.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
2201 (actual)
First submitted
1 Jun 2018
Start date
29 Jun 2018
Primary completion date
13 Mar 2025
Lead sponsor
Vastra Gotaland Region
NCT number
NCT03560310
EU CT number
2023-508551-40-00
EudraCT number
2017-001499-43

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 2201
  • From 29 Jun 2018 to the primary completion date, 13 Mar 2025
  • 22 sites in 5 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

  • Previously enrolled in this study (i.e. patient now at repeat encounter)
  • Concomitant surgical procedure other than CABG
  • Anticoagulant treatment after the operation (e.g. warfarin, direct thrombin inhibitors (dabigatran), FXa inhibitors (rivaroxaban, apixaban, heparin, low-molecular weight heparin, fondaparinux)
  • Any other indication for dual antiplatelet therapy, i.e. recent stent implantation
  • Debilitating stroke within 90 days before inclusion
  • Previous intracranial bleeding
  • Treatment with immunosuppressants (e.g. cyclosporine and tacrolimus)
  • Treatment with strong CYP3A4-inhibitors (e.g. ketoconazole, clarithromycin, nefazodone, ritonavir or atazanavir)
  • Participation in any other clinical trial evaluating investigational products at the time for enrollment in this study

Other illness

  • Any disorder that may interfere with drug absorption
  • Any condition other than coronary artery disease with a life expectancy \<12 months
  • Known chronic liver disease, renal disease requiring dialysis or bleeding disorder
  • Any condition that in the opinion of the investigator may interfere with adherence to trial protocol

Other

  • Discharge from the operating hospital to an ICU at another hospital
  • Pregnancy or lactation
  • Known intolerance or contraindication to ticagrelor or ASA
  • Atrioventricular block II and III in patients without pacemaker

Who the study is looking for

  • Written informed consent
  • Age ≥18 years
  • Has undergone first time isolated CABG due to an episode of acute coronary syndrome (STEMI, NSTEMI, unstable angina) within 6 weeks before surgery

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

Full criteria on ClinicalTrials.gov

Sites (22)

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

SiteCityCountrySite status
Aalborg University Hospital
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AalborgDenmarkActive, not recruiting
Aarhus Universitetshospital
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Aarhus NDenmarkActive, not recruiting
Rigshospitalet
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Copenhagen OeDenmarkActive, not recruiting
Odense University Hospital
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Odense CDenmarkActive, not recruiting
Meilahti Hospital
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HelsinkiFinlandActive, not recruiting
Kuopio University Hospital
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KuopioFinlandActive, not recruiting
Oulu University Hospital
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OuluFinlandActive, not recruiting
TAYS Sydaenkeskus Oy
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TampereFinlandActive, not recruiting
Turku University Hospital
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TurkuFinlandActive, not recruiting
Landspitali
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ReykjavikIcelandActive, not recruiting
Helse Bergen HF
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BergenNorwayActive, not recruiting
Oslo University Hospital HF
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OsloNorwayActive, not recruiting
Universitetssykehuset Nord-Norge HF
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TromsoeNorwayActive, not recruiting
St. Olavs hospital HF
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TrondheimNorwayActive, not recruiting
Sahlgrenska University Hospital-Vastra Gotalandsregionen
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GoteborgSwedenActive, not recruiting
Region Blekinge
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KarlskronaSwedenActive, not recruiting
Region Oestergoetland
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LinkopingSwedenActive, not recruiting
Region Skane Skanes Universitetssjukhus
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LundSwedenActive, not recruiting
Region Oerebro Laen
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OrebroSwedenActive, not recruiting
Karolinska University Hospital
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SolnaSwedenActive, not recruiting
Region Vaesterbotten
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UmeaSwedenActive, not recruiting
Uppsala University Hospital
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UppsalaSwedenActive, not recruiting

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