Status:
COMPLETED
Aspirin Dose and Atherosclerosis in Patients With Metabolic Syndrome
Lead Sponsor:
Florida Atlantic University
Collaborating Sponsors:
Bayer
Conditions:
Cardiovascular Diseases
Metabolic Syndrome X
Eligibility:
All Genders
40-80 years
Phase:
PHASE4
Brief Summary
The purpose of the study is to test higher versus lower doses of aspirin on markers of atherosclerosis in patients at risk of a first heart attack.
Detailed Description
Aspirin reduces risks of heart attacks, strokes, and deaths from cardiovascular causes in patients who have survived a prior event as well as during an acute heart attack. Aspirin also prevents a firs...
Eligibility Criteria
Inclusion
- 1\. Age 40 to 80 years, inclusive.
- 2\. No previous heart attack or a stroke, or other forms of these diseases.
- 3\. Have at least three of the five characteristics listed below, indicating presence of metabolic syndrome, as defined by NCEP-III:
- waist measuring more than 40 inches (for men) or more than 35 inches (for women),
- high density lipoprotein (HDL) cholesterol levels lower than 40 milligrams per deciliter (mg/dl) in men or 50 mg/dl in women,
- triglyceride (TG) levels above 150 mg/dl,
- blood pressure greater than 130 millimeters of mercury (mmHg) systolic or 85 mmHg diastolic,
- fasting blood sugar greater than 110 mg/dl
Exclusion
- Patients taking greater than 81mg aspirin daily.
- Patients taking anti-platelet drugs such as clopidogrel or non-steroidal anti-inflammatory drugs (NSAIDs) or anticoagulant drugs such as warfarin, during the last two weeks.
- Patients taking any of the following medications for less than 3 months, or who plan to take them for the first time during the next 3 months: ACE-inhibitors, angiotensin receptor blockers, calcium channel blockers, or statins.
- Patients who are currently cigarette smokers.
- Women patients who are pregnant, planning to become pregnant, nursing a child, or taking hormone replacement therapy.
- Patients with any coagulation, bleeding or blood disorders.
- Patients who are sensitive or allergic to aspirin.
- Patients with documented history of any gastrointestinal disorders, including bleeding ulcers.
- Patients with any evidence of cancer or history of significant cardiovascular disease (including heart attack, stroke or drop attacks termed transient ischemic attacks (TIAs), or blockages of the arteries in the legs termed peripheral arterial disease (PAD)), kidney, liver, lung, blood, or brain disorders.
- Patients with asthma, rhinitis, or nasal polyps.
- Patients with any abnormal laboratory value or physical finding that, in the view of the responsible clinician, may interfere with interpretation of the study results, be indicative of an underlying disease state, or compromise the safety.
- Patients with Class IV heart failure.
- Patients with severe aortic insufficiency, or aortic regurgitation.
- Patients with hearing loss or tinnitus.
- Patients with tremors which cause them not to be able to remain motionless for approximately 30 seconds.
Key Trial Info
Start Date :
October 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2009
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT00272311
Start Date
October 1 2006
End Date
January 1 2009
Last Update
February 27 2019
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
HeartDrug Research, LLC
Towson, Maryland, United States, 21204