Phase 4
N=25
Effects of Statin and Ezetimibe Association on Kinetics of Artificial Chilomicrons
Coronary Heart Disease
Bottom Line
View on ClinicalTrials.gov: NCT00481351 ↗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
| Outcome | Result | p-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.
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.