About this trial
To assess the rates of ischemic and hemorrhagic complications of long-term antithrombotic therapy in patients with chronic coronary syndromes
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
coronary artery disease , confirmed by history of myocardial infarction, or revascularization, or definitive evidence of CAD on imaging
Disqualifiers
Subjects who are unwilling or unable to provide informed consent.
Acute coronary syndrome within 12 months before inclusion
Severe chronic heart failure (NYHA IV)
Stroke within 6 months before inclusion
Trial population
Hospitalized or outpatients with confirmed chronic coronary syndromes
Trial design
Cohort
Prospective
Treatments tested in this trial
Antiplatelet Drug
Drugsingle or dual antiplatelets, triple antithrombotic therapy
Treatment groups
Trial outcomes
Primary outcomes
composite of major adverse cardiovascular events (MACE)
stroke, myocardial infarction, stent thrombosis \[definite or probable\], or urgent revascularization, cardiac death
composite of any bleeding events
major, clinically relevant nonmajor, minor (BARC, ISTH)
Secondary outcomes
Severity of peripheral atherosclerosis
Assessment will be performed with the use of duplex scanning
Mutations in following genes
CYP2C19\*, ABCB1
Sponsors and contacts
Click on the lead sponsor to view all of their trials.