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Cardiovascular Diseases clinical trials

View clinical trials related to Cardiovascular Diseases.

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NCT ID: NCT00005192 Completed - Hypertension Clinical Trials

Psychophysiology of Cardiovascular Reactivity

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

To determine why Black Americans have a higher prevalence of hypertension than whites by examining the interactions of psychosocial stressors and suppressed hostility with genetic or constitutional factors.

NCT ID: NCT00005191 Completed - Clinical trials for Cardiovascular Diseases

Clinical Course of Coronary Artery Disease Among Blacks

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

To determine the clinical course of coronary artery disease among Blacks receiving medical care for symptomatic heart diseases.

NCT ID: NCT00005190 Completed - Clinical trials for Cardiovascular Diseases

Reproduction and Survival After Cardiac Defect Repair

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

To create a registry of all Oregon children undergoing surgical repair of congenital heart disease since 1958 in order to determine mortality, morbidity, and disability after surgery and to assess the safety of pregnancy in women with corrected congenital heart disease and the risk of prematurity and occurrence of congenital heart defects in offspring.

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: NCT00005188 Completed - Clinical trials for Cardiovascular Diseases

Quantitative Genetic Analysis of Lipid Research Clinic Family Data

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

To assess the mode of inheritance of familial combined hyperlipidemia and familial primary hypoalphalipoproteinemia and to resolve genetic and familial environmental effects on several phenotypes of importance to coronary heart disease.

NCT ID: NCT00005187 Completed - Clinical trials for Cardiovascular Diseases

Cardiovascular Risk Profile Among Mexican-Americans

Start date: April 1986
Phase:
Study type: Observational

To characterize the epidemiology and genetics of apolipoproteins A-I, A-II, B, C-II, C-III, and E in a population of Mexican-Americans in Starr County, Texas.

NCT ID: NCT00005186 Completed - Clinical trials for Cardiovascular Diseases

Epidemiology of Cardiovascular Diseases in The Elderly

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

To identify and describe the distribution of risk factors for cardiovascular disease in a cohort of free-living elderly persons.

NCT ID: NCT00005185 Completed - Clinical trials for Cardiovascular Diseases

Myocardial Infarction and Non-contraceptive Estrogen Use

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

To evaluate whether the use of noncontraceptive estrogen influenced the incidence of first myocardial infarction in women.

NCT ID: NCT00005184 Completed - Obesity Clinical Trials

Immunogenetic Factors of Coronary Heart Disease

Start date: December 1985
Phase: N/A
Study type: Observational

To assess the association of immunogenetic factors with onset of coronary heart disease and the interrelationship of these factors with standard coronary heart disease risk factors.

NCT ID: NCT00005183 Completed - Clinical trials for Cardiovascular Diseases

Apolipoprotein A-I Gene Polymorphism and Atherosclerosis

Start date: December 1985
Phase: N/A
Study type: Observational

To further define the linkage of the Apo A-I gene polymorphism to genetic high density lipoprotein (HDL) deficiency and premature coronary artery disease. Also, to utilize this gene marker to define the prevalence of genetic HDL deficiency in patients with premature coronary disease and to determine the relative risk of premature coronary disease associated with the Apo A-I gene polymorphism.