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Heart Diseases clinical trials

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NCT ID: NCT00201162 Completed - Clinical trials for Cardiovascular Diseases

Soy and Lipoproteins in Postmenopausal Women

Start date: September 2001
Phase: N/A
Study type: Interventional

To determine the effects of soy on lipids, lipoproteins and lipoprotein subclass in a sample of African-American and white postmenopausal women with low-density lipoprotein (LDL) cholesterol elevations that may increase their lifetime risk for cardiovascular disease but would not qualify for definite pharmacotherapy under current guidelines.

NCT ID: NCT00201149 Completed - Hypertension Clinical Trials

Clinician Counseling and Cultural Competency to Improve Hypertension Control and Therapy Adherence

HCTA
Start date: February 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to test the effect of clinician counseling and cultural competence training on medication compliance and blood pressure (BP) control in patients with high BP.

NCT ID: NCT00201110 Completed - Clinical trials for Diabetes Mellitus, Type 2

Problem Solving and Cardiovascular Disease Risk Management in Diabetic Blacks

Start date: July 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to test a measurement tool and a new training intervention for problem solving in self-management of high cardiovascular disease (CVD) risk in African Americans with type 2 diabetes.

NCT ID: NCT00201084 Completed - Hypertension Clinical Trials

Physician Uncertainty Reduction for Hypertension

Start date: September 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to test the theory that a major factor in poor blood pressure (BP) control is that physicians fail to intensify antihypertensive therapy for their patients.

NCT ID: NCT00200993 Completed - Obesity Clinical Trials

Peripheral Effects of Exercise on Cardiovascular Health (STRRIDE I)

Start date: September 1998
Phase: Phase 2
Study type: Interventional

To investigate the separate effects of the amount of exercise and exercise intensity on cardiovascular risk factors in overweight men and women with mild to moderate dyslipidemia.

NCT ID: NCT00187889 Completed - Clinical trials for Ischemic Heart Disease

EWISE: Study of Eplerenone in Women With Chest Pain, Coronary Vascular Dysfunction and Evidence of Myocardial Ischemia

Start date: August 2004
Phase: Phase 4
Study type: Interventional

Some women have chest pain even without having a blockage in one of the major blood vessels that supplies blood to the heart. In many of these women the microscopic (small) blood vessels in the heart do not function normally. This study seeks to determine if treatment with eplerenone, a commercially available diuretic, can improve the function of these microscopic blood vessels and, possibly, improve the chest pain.

NCT ID: NCT00187213 Completed - Heart Failure Clinical Trials

B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Cardiac Defibrillator (ICD) Back-Up in Heart Failure Patients

Start date: December 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate that biventricular pacing (BiV) and left univentricular (left ventricular [LV] only) pacing are safe and effective for cardiac resynchronization therapy in heart failure patients implanted with a cardiac resynchronization therapy defibrillator (CRT-D) device. The hypothesis to be tested by this clinical investigation is that patients indicated for an ICD with cardiac resynchronization therapy respond as well to LV only pacing as to BiV pacing.

NCT ID: NCT00185978 Completed - Obesity Clinical Trials

Obesity Prevention for Pre-Adolescents

Start date: April 1998
Phase: Phase 2
Study type: Interventional

To develop and evaluate, in a randomized controlled trial, a comprehensive obesity prevention program for third, fourth and fifth grade students. The intervention includes activities in THE SCHOOL, THE HOME, and a clinically oriented component for HIGH-RISK CHILDREN. In addition, the intervention will be delivered over a 3 year period, with age and grade-appropriate components for 3rd, 4th and 5th graders and their families. The primary outcome is body mass index. PRIMARY OBJECTIVE: To significantly reduce body mass index, compared to controls, at the end of the three year intervention.

NCT ID: NCT00185250 Completed - Heart Diseases Clinical Trials

Betaferon/ Betaseron (Interferon Beta-1b) in Patients With Chronic Viral Cardiomyopathy

Start date: December 2002
Phase: Phase 2
Study type: Interventional

Chronic viral cardiomyopathy is a disease where the cardiac muscle is attacked by a virus and this may result in a reduction in the output of the heart (pump function) thereby causing complaints such as chest pain, shortness of breath and palpitations. Betaferon (interferon beta-1b) is marketed for the treatment of Multiple Sclerosis already, but until now, it has not been proven whether it is also effective in patients with chronic viral myocardial disease. This study will be conducted to examine the efficacy and safety of Betaferon in patients with this disease. The aim of the treatment is to eliminate the virus from the heart so that the heart function and clinical status can gradually improve.

NCT ID: NCT00182949 Completed - Heart Disease Clinical Trials

Genetics and Epidemiology of Aging Associated Conditions in the Sardinian Population

Start date: November 19, 2003
Phase:
Study type: Observational

Background: - The island of Sardinia, an Italian region, has a population that is highly interrelated. Researchers have developed the SardiNIA longitudinal study to examine the possible genetic factors that predispose individuals to diseases and to various inherited conditions. In the study, participants will be drawn from four towns in the Ogliastra region (Lanusei, Ilbono, Elini, and Arzana), and their DNA will be analyzed and compared with a long-term assessment of various health-related events. The SardiNIA study is designed to improve understanding of the genetic factors involved in age-associated diseases and disorders, and provide possible points of intervention that may help prevent diseases. Objectives: - To conduct a long-term study of genetics and epidemiology in a small and highly interrelated population. Eligibility: - Individuals at least 18 years of age (at least 14 years of age for Phase 1 of the study) who live in the province of Ogliastra in eastern Sardinia. Design: - This 10-year study will involve three phases: collecting initial blood samples and medical history (years 1 to 4), and two sets of follow-up visits to collect additional data (3 years apart). - Participants will provide detailed medical history and information for long-term study, primarily involving the following aspects: - Demographic/family and clinical variables (e.g., medications, fertility, hospitalizations and surgical procedures, age of relatives who are still alive, age and cause of death in deceased relatives) (Phase 1) - Complete physical examination, including measures of height and weight, blood pressure, and basic heart function (Phase 1) - Blood and urine samples (Phase 1) - Heart and lung function tests (Phase 1) - Assessment of general personality traits and possible history of depression (Phase 1) - Dietary assessment through a food frequency questionnaire (Phase 1) - Cognitive tests of attention, memory, and concentration (Phases 1 and 2) - Frailty-related tests (e.g., hand grip strength, walking speed, bone strength) (Phases 1 and 2) - Eye examination to test for evidence of disease or macular degeneration (Phases 1 and 2) - Kidney and thyroid ultrasound (Phases 1, 2, and 3)