Remote Ischemic Conditioning to Attenuate Myocardial Death and Improve Operative Outcome. (RICARDO)
Coronary Artery Bypass, Myocardial Reperfusion Injur, Ischemic Preconditioning, Myocardial

About this trial
This is an interventional treatment trial for Coronary Artery Bypass focused on measuring myocardial protection, remote ischemic preconditioning, remote ischemic postconditioning, cardiac surgery
Eligibility Criteria
Inclusion Criteria:
Patients qualified to coronary artery bypass grafting according to ESC/EACTS Guidelines of myocardial revascularization, suffering from:
- Multivessel coronary artery disease amenable for surgical treatment
- Negative history of previous cardiac or vascular surgery in childhood and afterwards.
- Negative history of active neoplastic disease, neither past medical history of oncological treatment
- Patients with non insulin dependent diabetes mellitus treated chronically with oral derivatives of sulfonylourea such as but not limited to: glibenclamide.
Exclusion Criteria:
Patients suffering from acute insuficiency of any organ/ system and those suffering from end stage organ failure such as:
- Chronic renal disease - KDOQI stage ≥ 3;
- Chronic renal failure class A by Child - Pugh'a;
- Chronic respiratory failure (type I and II according to Campbell et al. and type I according to Wood et al.);
- Chronic intermittent claudication class 2A according to Fontaine;
Sites / Locations
- Medinet Heart CentreRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
RIC Group
Control Group
Three cycles of remote ischemic conditioning (5minutes ischemia and 5minutes reperfusion; lower leg ischemia achieved by pressure cuff inflation and deflation); First three cycles the patient will receive 24 hours preoperatively, second three cycles the patient will receive after the induction of general anesthesia but before skin incision shortly before CABG. Remote ischemic postconditioning (5minutes ischemia and 5minutes reperfusion; lower leg ischemia achieved by pressure cuff inflation and deflation) will be administered to the patient within 60 minutes after the completion of all coronary artery bypass grafts and the restoration of coronary blood flow.
Control group will receive sham procedure near identical to intervention. That will be afforded by inflation of pressure cuff on artificial leg hidden under the draping by an assistant who is not included in the research team and does not have any connection to study design and data analysis.