Remote Ischemic Preconditioning in Type 2 Diabetic Patients Undergoing CABG

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-85
SponsorMuğla Sıtkı Koçman University

About this trial

This randomized, double-blind, prospective clinical trial aims to investigate the effect of remote ischemic preconditioning (RIPC) on myocardial protection in patients with type 2 diabetes mellitus undergoing elective coronary artery bypass graft (CABG) surgery. Perioperative myocardial injury remains a significant concern during CABG, particularly in high-risk patients such as those with diabetes. RIPC is a low-cost, non-invasive intervention that may reduce myocardial damage by enhancing ischemic tolerance through intermittent limb ischemia.

Sixty patients aged 40-85 years with type 2 diabetes scheduled for isolated CABG will be randomized to either receive RIPC or standard care. RIPC will be applied through five cycles of upper limb cuff inflation and deflation prior to sternotomy. High-sensitivity troponin T levels will be measured at 24, 48, and 72 hours postoperatively to assess myocardial injury. Secondary outcomes include acute kidney injury (KDIGO classification), maximum vasoactive-inotropic score (VIS) during the first 72 postoperative hours, ICU and hospital length of stay. This study will provide insight into the cardioprotective role of RIPC in diabetic patients undergoing cardiac surgery.

Eligibility criteria

Qualifiers

Diagnosed with type 2 diabetes mellitus and receiving medical treatment

Scheduled for isolated elective coronary artery bypass graft (CABG) surgery

American Society of Anesthesiologists (ASA) physical status class III or IV

Age between 40 and 85 years

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Remote Ischemic Preconditioning

Treatment groups

60 Participants
are divided into 2 treatment groups