← Eichor
Study identifier: NCT06977230 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Remote Ischemic Preconditioning in Type 2 Diabetic Patients Undergoing CABG

Condition: Diabetes Mellitus · Coronary Artery Bypass · Remote Ischaemic Conditioning  ·  Sponsor: Muğla Sıtkı Koçman University

PhaseNA
Planned participants60
Who can joinAll sexes, 45 Years to 85 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Melike Korkmaz Toker, Associate Professor  ·  00905054747098  ·  meltoker@gmail.com

Always discuss trial participation with your own doctor first.

Locations (2)

Mugla Training and Research HospitalMuğla, Turkey (Türkiye)Not Yet Recruiting
Mugla Training and Research HospitalMuğla, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06977230