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
- Diseases
- Coronary artery disease
- 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
Sites (22)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Aalborg University Hospital Coordinator of this site? Confirm its status | Aalborg | Denmark | Active, not recruiting |
| Aarhus Universitetshospital Coordinator of this site? Confirm its status | Aarhus N | Denmark | Active, not recruiting |
| Rigshospitalet Coordinator of this site? Confirm its status | Copenhagen Oe | Denmark | Active, not recruiting |
| Odense University Hospital Coordinator of this site? Confirm its status | Odense C | Denmark | Active, not recruiting |
| Meilahti Hospital Coordinator of this site? Confirm its status | Helsinki | Finland | Active, not recruiting |
| Kuopio University Hospital Coordinator of this site? Confirm its status | Kuopio | Finland | Active, not recruiting |
| Oulu University Hospital Coordinator of this site? Confirm its status | Oulu | Finland | Active, not recruiting |
| TAYS Sydaenkeskus Oy Coordinator of this site? Confirm its status | Tampere | Finland | Active, not recruiting |
| Turku University Hospital Coordinator of this site? Confirm its status | Turku | Finland | Active, not recruiting |
| Landspitali Coordinator of this site? Confirm its status | Reykjavik | Iceland | Active, not recruiting |
| Helse Bergen HF Coordinator of this site? Confirm its status | Bergen | Norway | Active, not recruiting |
| Oslo University Hospital HF Coordinator of this site? Confirm its status | Oslo | Norway | Active, not recruiting |
| Universitetssykehuset Nord-Norge HF Coordinator of this site? Confirm its status | Tromsoe | Norway | Active, not recruiting |
| St. Olavs hospital HF Coordinator of this site? Confirm its status | Trondheim | Norway | Active, not recruiting |
| Sahlgrenska University Hospital-Vastra Gotalandsregionen Coordinator of this site? Confirm its status | Goteborg | Sweden | Active, not recruiting |
| Region Blekinge Coordinator of this site? Confirm its status | Karlskrona | Sweden | Active, not recruiting |
| Region Oestergoetland Coordinator of this site? Confirm its status | Linkoping | Sweden | Active, not recruiting |
| Region Skane Skanes Universitetssjukhus Coordinator of this site? Confirm its status | Lund | Sweden | Active, not recruiting |
| Region Oerebro Laen Coordinator of this site? Confirm its status | Orebro | Sweden | Active, not recruiting |
| Karolinska University Hospital Coordinator of this site? Confirm its status | Solna | Sweden | Active, not recruiting |
| Region Vaesterbotten Coordinator of this site? Confirm its status | Umea | Sweden | Active, not recruiting |
| Uppsala University Hospital Coordinator of this site? Confirm its status | Uppsala | Sweden | Active, not recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.