Effect of Adding Vildagliptin vs Glimepiride to Metformin on Inflammation's Markers in Type-2 Diabetic Patients With CAD

The study is designed as a single-center, randomized, double-blinded, clinical trial to provide evidence on the effects of vildagliptin on key biomarkers of atherothrombosis and inflammation. The investigators plan to prospectively enroll 80 patients with proven coronary artery disease ,Diabetes type2 and randomize them in a 1:1 ratio to either vildagliptin-metformin therapy (n=40) or glimepiride /metformin therapy (n=40).

• All participants agreed to take part in this clinical study and provide informed consent.
• Patients with Coronary artery diseases.and uncontrolled Diabetes type2 who's taking metformin only will be enrolled (n=80) from endocrinology clinic at Alexandria Armed Forces hospital.
• Complete physical, laboratory, radiological assessment will be done for all patients to exclude any signs of inflammation or thrombosis.
• Serum samples will be collected for measuring the biomarkers.
• All enrolled patients will be mentioned as two groups; Group I (n=40) are patients who the endocrinologist prescribed them vildagliptin plus their metformin to control their blood sugar level. Group II (n=40) are patients who the endocrinologist prescribed them glimepiride plus their metformin.
• All patients will be followed up during 3 months' period.
• At the end of 3 months on the new regimen, steps 4 and 5 will be repeated.
• Statistical tests appropriate to the study design will be conducted to evaluate the significance of the results.
• Measuring outcome: The primary outcome is the change of serum levels of the measured inflammatory markers after 3 months.
• Results, conclusion, discussion and recommendations will be given.

Inclusion criteria

• Adult patients with Type II-diabetes mellitus on metformin who are planned to be managed with vildagliptin or glimepiride plus metformin at the time of inclusion.
• Symptomatic Coronary Artery Diseases. (>30 days).

Exclusion criteria

• Hepatic impairment.
• Active malignancy.
• Planned surgical intervention.
• Any signs of hypersensitivity or contraindication to study drugs developed.
• Any patient with any signs of active infection or thrombosis at the time of assessment.
• Addition of any antidiabetic medications or insulin during follows up.
• Chronic inflammatory disease (i.e. inflammatory bowel disease, lupus, inflammatory arthritis, rheumatoid arthritis) or chronic infection (i.e. chronic diabetic foot infection).
• Clinically advanced congestive heart failure - New York Heart Association III-IV
• Severe left ventricular dysfunction (LVEF<30%) with New York Heart Association II or any New York Heart Association class with documented recent heart failure decompensation (<3 months)
• Severe stable cardiac angina Community Competence Scale III - IV or Unstable angina
• Pregnancy, lactation or child-bearing potential.