About this trial
PROFILE-HF is a multicenter, observational, prospective study of the clinical course and outcomes of chronic heart failure (HF) and coronary artery disease (CAD) in patients undergoing coronary artery bypass grafting (CABG).
The objective of the study is to develop a method for assessing the risk of adverse cardiovascular events in patients with CAD and HF who have undergone CABG, based on preoperative GDF-15 concentrations.
The study will have a 12-month follow-up period; one in-person visit is planned at the end of the follow-up period. If it is not possible to visit a doctor in person, information will be collected through telephone contact with the patient or his relative or person caring for the patient.
Eligibility criteria
Qualifiers
Heart Failure
Planned coronary artery bypass grafting
Disqualifiers
Myocardial infarction
Stroke
Presence of implanted devices;
Need for additional cardiac surgery other than coronary artery bypass grafting (valve repair, aneurysm);
Trial design
Treatments tested in this trial
- Not listed