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Search / Trial NCT06977230

Remote Ischemic Preconditioning in Type 2 Diabetic Patients Undergoing CABG

Launched by MUĞLA SITKI KOÇMAN UNIVERSITY · May 14, 2025

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

High Sensitive Troponin T Diabetes Mellitus Type 2 Coronary Artery Bypass Myocardial Ischemia Remote Ischemic Conditioning Acute Kidney Injury Cardioprotection

ClinConnect Summary

This clinical trial is looking at a technique called remote ischemic preconditioning (RIPC) to see if it can help protect the heart during surgery for patients with type 2 diabetes who are having coronary artery bypass graft (CABG) surgery. The study is important because people with diabetes are at higher risk for heart damage during this type of surgery. RIPC is a simple and safe method that involves using a cuff on the arm to temporarily restrict blood flow. This may help the heart better tolerate the stress of surgery.

To participate in the trial, patients must be between 40 and 85 years old, have type 2 diabetes that is being treated, and be scheduled for elective CABG surgery. Those who have certain health issues, such as severe heart problems or kidney failure, will not be eligible. If patients join, they will either receive RIPC before their surgery or standard care. Researchers will monitor their heart health after surgery to see if RIPC makes a difference in reducing heart injury and other complications. This study aims to understand how RIPC might help improve outcomes for diabetic patients undergoing heart surgery.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 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
  • Exclusion Criteria:
  • Emergency CABG surgery Reoperation (revision surgery) Left ventricular ejection fraction (LVEF) \< 40% History of cardiac arrest or cardiogenic shock Pregnancy Clinically significant peripheral arterial disease affecting the upper limbs Hepatic dysfunction (bilirubin \> 20 μmol/L or INR \> 2.0) Renal failure (eGFR \< 20 mL/min/1.73 m²) Ongoing treatment with glibenclamide or nicorandil (agents known to interfere with ischemic preconditioning mechanisms) Asthma

About Muğla Sıtkı Koçman University

Muğla Sıtkı Koçman University is a distinguished academic institution located in Turkey, committed to advancing research and innovation in various fields, including health sciences. As a clinical trial sponsor, the university leverages its robust research infrastructure and expertise to facilitate high-quality clinical studies that aim to enhance medical knowledge and improve patient outcomes. With a focus on ethical practices and collaboration, Muğla Sıtkı Koçman University strives to contribute significantly to the scientific community through rigorous clinical research and development initiatives.

Locations

Mugla, , Turkey

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported