Actively Recruiting
Coronary CT Angio Evaluating Graft Patency in ACS Patients Treated With DAPT or Single ASA After CABG (CoCAP)
Led by University Hospital, Linkoeping · Updated on 2025-12-19
360
Participants Needed
6
Research Sites
251 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to compare the presence of graft patency in single aspirin vs dual anti platelet therapy (DAPT) treatment including ticagrelor in patients with acute coronary syndrome (ACS) treated with coronary artery bypass surgery (CABG). Follow up time is 12-36 months postoperatively and the patency will be evaluated with coronary computed tomography angiography (CCTA)
CONDITIONS
Official Title
Coronary CT Angio Evaluating Graft Patency in ACS Patients Treated With DAPT or Single ASA After CABG (CoCAP)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Previously included in TACSI-trial
You will not qualify if you...
- Highly irregular heart rhythm (i.e. atrial fibrillation)
- Chronic kidney disease with estimated glomerular filtration rate (eGFR) <45ml/min/1,73m2
- Body weight >120 kg
- Previous severe allergic reaction (i.e. anaphylactic reaction) to iodine-based contrast agents
- Not able to communicate
- Not willing to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 6 locations
1
Department of Heart Disease, Haukeland University Hospital
Bergen, Norway
Enrolling by Invitation
2
St Olavs University Hospital
Trondheim, Norway
Not Yet Recruiting
3
Department of Molecular and Clinical Medicine, Wallenberg Laboratory, Institute of Medicine
Gothenburg, Sweden
Enrolling by Invitation
4
Dep of Vascular and Thoracic Surgery
Örebro, Sweden
Active, Not Recruiting
5
Department of Cardiothoracic Surgery Karolinska University Hospital
Stockholm, Sweden
Enrolling by Invitation
6
University Hospital Linköping
Linköping, Östergötland County, Sweden, 58185
Actively Recruiting
Research Team
J
Jonas Holm, MD, PhD
CONTACT
S
Sofia Sederholm Lawesson, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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