Mode
Text Size
Log in / Sign up
Phase 4 N=25 Randomized Treatment

Effects of Statin and Ezetimibe Association on Kinetics of Artificial Chilomicrons

Coronary Heart Disease

Enrolled (actual)
25
Serious AEs
Results posted
Jan 2011
Primary outcome: Primary: Cholesteryl Ester Fractional Clearance Rate

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Simvastatin 20mg plus ezetimibe 10mg (Drug); ezetimibe (Drug); simvastatin 20mg (Drug); Simvastatin 80mg (Drug)
Age
Adult, Older Adult · 30+ yrs
Sex
All
Sponsor
University of Sao Paulo
Primary completion
Jan 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Cholesteryl Ester Fractional Clearance Rate
PRIMARY
Low Density Lipoprotein
74.85; 71.92
SECONDARY
Triglyceride Fractional Clearance Rate
SECONDARY
Alanine Aminotransferase
30.46; 18.33
SECONDARY
CPK
169; 131
SECONDARY
Total Cholesterol
152.61; 148.29
SECONDARY
High Density Lipoprotein
51.31; 44.33

Summary

Effects of statin and ezetimibe association on kinetics of artificial chylomicrons in men with stable coronary heart disease (CHD). Background: The rate (kinetics) of chylomicrons removal from circulation have been correlated with the incidence and severity of atherosclerotic lesions; a number of studies demonstrated lower plasmatic clearance of chylomicrons in patients with CHD compared to patients without this condition. It was also demonstrated a correlation among LDL-C levels and removal of chylomicrons remnants by a technique employing artificial chylomicrons. The investigators also know that higher doses of more potent statins are more effective in chylomicrons removal than lower doses or less potent statins; nevertheless, the effect of the isolated use of statin has not been completely studied up to now. Study design: The investigators propose to study 26 outpatients volunteers with chronic CHD, followed at the Heart Institute - INCOR - of the School of Medicine, University of São Paulo. Following a period of six weeks of washout from any cholesterol reducer, the kinetics of chylomicrons removal by a technique of emulsion of radiolabeled artificial chylomicrons will be evaluated. Lipid fractions, hepatic enzymes and CK will be measured. Initially patients will be randomly allocated to receive simvastatin 20 mg /day (n= 13) or ezetimibe 10 mg/day (n=13) for six weeks. At the end of this period, kinetics of chylomicrons removal and laboratorial measurements will be repeated (Period 1). In the next period (Period 2) patients will receive simvastatin 20 mg/ ezetimibe 10 mg (n=13) or simvastatin 80 mg (n=13) for additional six weeks; at the end of this period, the evaluations will be repeated (third and last evaluation). The aim of this study is to further understand chylomicrons metabolism in patients with chronic coronary disease receiving cholesterol reducers at different dosage regimes.

Eligibility Criteria

Inclusion Criteria

  • Stable coronary heart disease.

Exclusion Criteria

  • Renal and Liver failure
  • Hypothyroidism
  • Diabetes mellitus
  • Neoplasia
  • Heart failure.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00481351). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search