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Carotid Artery Diseases clinical trials

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NCT ID: NCT00005263 Completed - Clinical trials for Cardiovascular Diseases

Postprandial Lipoproteins and Atherosclerosis

Start date: July 1990
Phase: N/A
Study type: Observational

To determine whether postprandial lipoproteins were associated with atherosclerosis, and if so, whether the association was statistically independent of that between fasting lipoproteins and atherosclerosis.

NCT ID: NCT00005260 Completed - Clinical trials for Cardiovascular Diseases

Mechanisms Underlying Psychosocial Associations With Ischemic Heart Disease (Kuopio)

Start date: July 1990
Phase: N/A
Study type: Observational

To examine the relationships among psychosocial factors and carotid atherosclerosis, myocardial ischemia, arrhythmias, and thrombosis.

NCT ID: NCT00005230 Completed - Hypertension Clinical Trials

Epidemiology of Carotid Disease in Elderly Adults

Start date: July 1988
Phase: N/A
Study type: Observational

To determine whether a population with isolated systolic hypertension (ISH) had a higher prevalence of carotid disease than a normotensive population matched for age and sex, and to determine specific risk factors for carotid disease.

NCT ID: NCT00005189 Completed - Clinical trials for Cardiovascular Diseases

Carotid Atherosclerosis Follow-up Study

Start date: July 1986
Phase: N/A
Study type: Observational

To determine whether the degree of carotid artery atherosclerosis, as measured by B-mode ultrasound, predicts the development of myocardial infarction, stroke, and all-cause mortality in patients with angiographically defined coronary status. Also, to quantify the rate of progression of carotid artery disease and to evaluate the risk factors associated with progression of carotid atherosclerosis.

NCT ID: NCT00005160 Completed - Depression Clinical Trials

Epidemiology of Cardiovascular Risk Factors in Women (Healthy Women Study)

Start date: April 1983
Phase: N/A
Study type: Observational

To determine cardiovascular risk factors and the change in risk factors during and following the menopause.

NCT ID: NCT00005134 Completed - Obesity Clinical Trials

Strong Heart Study

Start date: September 1988
Phase: N/A
Study type: Observational

To determine morbidity and mortality from cardiovascular disease among American Indians and to compare cardiovascular disease risk factor levels among Indian groups living in different geographic areas.

NCT ID: NCT00001589 Completed - Clinical trials for Myocardial Infarction

Comparison of Asymptomatic Carotid Atherosclerosis Between Frequent and Infrequent Blood Donors

Start date: April 1997
Phase: N/A
Study type: Observational

Iron has been proposed to contribute to atherogenesis in humans by facilitating the oxidation of lipoproteins. This observational study will evaluate the association between frequency of blood donation - expected to be associated with relatively reduced body iron stores in frequent donors - and carotid atherosclerosis. The primary outcome variable will be whether the presence and extent of asymptomatic carotid atherosclerosis as measured by ultrasound is greater in infrequent (less than or equal to 1 donations/year greater than or equal to 5 years) vs. frequent (greater than or equal to 4 donations/year greater than or equal to 5 years) blood donors. Body iron stores, lipid and hemostatic parameters, nitric oxide formation, inflammatory parameters, and markers of vascular oxidative stress will be analyzed as secondary outcome measures. Laboratory analysis and ultrasound testing will be performed blinded to the patient's phlebotomy and iron status. Sixty frequent (n=40 males greater than 40 y/o, n=20 females greater than 50 y/o) and 60 infrequent (n=40 males greater than 40 y/o, n=20 females greater than 50 y/o) blood donors will be recruited for this study from the Department of Transfusion Medicine, W. G. Magnuson Clinical Center. All donors will be assessed for study eligibility and cardiovascular risks during the screening visit. The presence of atherosclerotic lesions by carotid ultrasound and secondary outcome parameters will be assessed during a second visit.

NCT ID: NCT00001368 Completed - Hypertension Clinical Trials

Potential Risk Factors for Stroke

Start date: October 1993
Phase: Phase 1
Study type: Interventional

Early studies have shown that the immune system may play a role in the development of strokes. Conditions such as high blood pressure, high cholesterol, diabetes, and old age can activate the immune system and increase the risk of developing hardening of the arteries (atherosclerosis) and damaged blood vessels. Researchers will attempt to characterize factors that may contribute to atherosclerosis and stroke by measuring certain components of the immune system, cytokines and leukocyte activation. Measurements will be taken from patients that are considered to be stroke prone and from patients without risk factors for the development of stroke. Researchers will measure the immune system components at the beginning of the study, at six months, and at the one-year completion of the study. The study will attempt to determine; I) If patients with risk factors for stroke have an increased activation of the immune system II) If patients with risk factors for stroke that are symptomatic have higher levels of immune system activation compared to patients who do not have symptoms III) If patients with increased activation of the immune system have accelerated hardening of the arteries (atherosclerosis)

NCT ID: NCT00000600 Terminated - Clinical trials for Cardiovascular Diseases

Vitamin E and C to Slow Progression of Common Carotid Artery Plaque Build-Up

Start date: June 1995
Phase: Phase 2
Study type: Interventional

This study will evaluate the effects of vitamin E supplementation in retarding the progression of common carotid artery intima-media thickening in African Americans.

NCT ID: NCT00000599 Completed - Clinical trials for Cardiovascular Diseases

Cholesterol-Lowering Atherosclerosis Study (CLAS)

Start date: June 1980
Phase: Phase 3
Study type: Interventional

To determine whether combined therapy with the lipid lowering agents colestipol hydrochloride plus niacin would produce significant change in coronary, carotid, and femoral artery atherosclerosis and coronary bypass graft lesions as determined by angiography. Also, to determine possible correlations between lesion changes and plasma lipid and lipoprotein cholesterol levels and to explore interrelationships of atherosclerosis change in femoral, coronary, and carotid arteries.