Overview

Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inflammatory Mediators and Thrombosis

Status:
Completed
Trial end date:
2002-04-01
Target enrollment:
0
Participant gender:
All
Summary
This is a randomized placebo controlled clinical trial designed to investigate the effects of micronized fenofibrate on fasting and postprandial lipoproteins, oxidized fatty acids and lipoproteins, inflammatory mediators and thrombotic factors among hypertriglyceridemic individuals with two or more other characteristics of the metabolic syndrome.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Michigan
Collaborator:
Abbott
Treatments:
Fenofibrate
Criteria
Inclusion Criteria:

1. males and postmenopausal females 18 years of age with fasting triglycerides greater
than or equal to 1.7 mmol/L and <6.9 mmol/L

2. two or more of the following Adult Treatment Panel III (1) criteria of the metabolic
syndrome: abdominal obesity (waist circumference >89 cm in females and >102 cm in
males); low high-density lipoprotein cholesterol (HDL-C) (<1.3 mmol/L in women and
<1.0 mmol/L in men); hypertension (systolic blood pressure >130 or diastolic blood
pressure >85 mm Hg) or current drug therapy for hypertension; and impaired fasting
glucose (between 6.1 mmol/L and 7.0 mmol/L).

Exclusion Criteria:

1. included types 1 or 2 diabetes

2. Body mass index >40 kg/m2

3. Use of lipid-lowering therapies

4. Oral hypoglycemic therapies

5. Insulin

6. Aspirin >81 mg daily

7. Regular use of non-steroidal anti-inflammatory agents or cyclooxygenase-2 inhibitors,
corticosteroids (oral and inhaled), anti-oxidants (including multivitamins), herbal or
fiber supplements recent changes in type or formulation of hormone replacement therapy
(in the last 6 months)

8. Alcohol intake >3 drinks per day

9. Untreated hypothyroidism or recent change (within 2 months) of thyroid replacement
therapy

10. Cigarette smoking (current or within the last 6 months)