Overview

Effect of Fenofibrate on Endothelial Function and High-density Lipoproteins (HDL)in Patients With Coronary Heart Disease

Status:
Completed
Trial end date:
2011-01-01
Target enrollment:
0
Participant gender:
Male
Summary
Fenofibrate is a drug that acts on the PPAR alpha receptors, increasing HDL-cholesterol and decreasing triglyceride levels. The interaction with these receptors has antiatherogenic actions by regulating the expression con key proteins that participate in vascular inflammation, plaque stability and thrombosis. Fenofibrate reduces triglycerides and increases HDL-C in plasma. It also decreases small, dense LDL particles. The use of this drug has resulted in improvement of vascular function measured by endothelial function. Our hypotheses state that fenofibrate will improve: endothelial function, improve HDL antioxidant capacity and size distribution towards a predominance of small HDL particles.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
National Heart Institute, Mexico
Treatments:
Fenofibrate
Criteria
Inclusion Criteria:

- Male patients 18-60 years of age

- Stable coronary heart disease (no cardiovascular event 3 months prior to enrollment)

- Stable lipid-modifying drug therapy (previous 2 months)

- Low-dose statin therapy with LDL-C at goal (< 100 mg/dl)

- Triglyceride levels 151-500 mg/dl

- HDL-C levels <40 mg/dl

Exclusion Criteria:

- Diabetes mellitus

- Uncontrolled hypertension Systolic blood pressure >160 mmHg and/or diastolic blood
pressure >100 mmHg

- Subjects with renal (serum creatinine >1.5 times the upper limit of normal (ULN)),
hepatobiliary (cholelithiasis, biliary cirrhosis, AST and/or ALT >2x ULN) or active
thyroid disease (TSH >1.5x ULN or <0.05 uUI/ml)

- Hypersensitivity to fenofibrate or to any other component of its formula

- History of photoallergic reaction or phototoxicity to fenofibrate or ketoprofen