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Heart Diseases clinical trials

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NCT ID: NCT00918242 Recruiting - Clinical trials for Coronary Heart Disease

Prevalence of Coronary Artery Disease in the Siblings of Premature Coronary Heart Disease

Start date: June 2009
Phase: N/A
Study type: Observational

The aim of this prospective study is to investigate the prevalence of coronary artery disease using computed tomography with family history of premature coronary heart disease

NCT ID: NCT00917527 Recruiting - Clinical trials for Coronary Heart Disease

Endothelial Dysfunction in Subjects With History of Premature Coronary Artery Disease

Start date: June 2009
Phase: Phase 4
Study type: Interventional

The aim of this prospective study is to investigate the prevalence of endothelial dysfunction in subjects with family history of premature coronary heart disease. At the same time, the effect of atorvastatin in treating subclinical endothelial dysfunction in those patients will be evaluated.

NCT ID: NCT00875173 Recruiting - Chagas Disease Clinical Trials

Selenium Treatment and Chagasic Cardiopathy (STCC)

STCC
Start date: October 2008
Phase: Phase 3
Study type: Interventional

Background: Chagasic myocardiopathy caused by the protozoa Trypanosoma cruzi has been the principal cause of cardiac death in Latin America. Without any trypanocidal therapeutic intervention, infected subjects can pass from the indeterminate to the cardiac form with heart dysfunction. Our group has studied the role and the effect of the supplementation with the essential micronutrient selenium (Se) on T. cruzi infection, and the investigators have verified that: 1. low Se levels is related to the severity of the myocardiopathy in chagasic patients 2. adequate Se diet is essential for mice survival at the acute phase of the experimental T. cruzi infection 3. Se supplementation prevented the myocardial lesions at the acute phase in mice. From these findings and considering that Se supplementation was able to prevent Keshan cardiopathy, to revert electrocardiographic and echocardiographic alterations in patients nourished by parenteral route, and reduced re-infarction and cardiac deaths from acute myocardial infarction; the investigators purpose to investigate if Se treatment via oral route, is able to impair the progress of heart dysfunction in chagasic patients expressed by the study of progression rate and by the comparison of the means of ventricular ejection fraction. Methods: The Selenium treatment and Chagasic Cardiopathy (STCC) trial is double-blind, placebo controlled, randomized in 130 chagasic patients at the chronic phase following the inclusion criteria of (a) altered ECHO (LVEF between 0,35 % and 45 %), (b) age between 20 and 65 years, (c) randomly divided in two groups: Placebo (n=65) and Se (n=65). Patients of Se group will intake diary 100 µg Se as sodium selenite for 12 months. The primary endpoint is the reduction of 50 % in the progression rate of heart dysfunction, and the secondary endpoint is a partial or total reversion in electrocardiography alterations. Conclusion: This trial was recently approved by Brazilian Research Ethics Committee and will be conducted in accordance with the principles for human experimentation. If the investigators confirmed the benefit of Se treatment, a strategy of utilization a micronutrient in an adequate concentration as a treatment in diary diet can revolutionize the therapeutic for chagasic myocardiopathy.

NCT ID: NCT00868829 Recruiting - Clinical trials for Coronary Heart Disease

Firebird2 Cobalt-Chromium Alloyed Sirolimus-Eluting Stent Registry Trial

FOCUS
Start date: April 2009
Phase: N/A
Study type: Interventional

The experimental design is a multi-center, prospective, non-controlled, non-randomized, single-arm clinical registry trial. The study will enroll 5,000 patients who receive the Firebird2TM Cobalt-ChromiumAlloyed Sirolimus-Eluting Stent implantation. For patient with multivessel disease, only Firebird 2TM Stent will be implanted. The enrollment of patients will take about 4 months. Clinical follow-up will be at 30 day, 6 month, 12 month, 24 month and 36 month. Patients withdrawing the study due to any reasons will not be replaced.

NCT ID: NCT00850486 Recruiting - Clinical trials for Ischemic Heart Disease

Diagnostic Benefits of HyperQTM vs. Conventional ECG Stress Test. Comparison of HyperQ vs. Stress ECG in Women Before Angiography

Start date: August 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to verify the efficiency of the HyperQ technology compared with standard ECG analysis in detecting exercise induced ischemia in women who are referred to coronary angiography.

NCT ID: NCT00830726 Recruiting - Heart Failure Clinical Trials

Water- and Salt-homeostasis in Healthy Humans, and in Patients With Heart- or Lung Disease

Start date: February 2009
Phase: N/A
Study type: Observational

The purpose of the study is to determine whether the excretion of renal water- and salt-channels in the urine reflects the handling of water and salt in the kidneys, and whether the excretion can be used to monitor and/or predict the effects of treatment of certain heart or lung diseases.

NCT ID: NCT00772135 Recruiting - Clinical trials for Congenital Heart Disease

Reversibility by Sildenafil of Exercise-Induced Abnormal Right Ventricular Pressure Response in ASD and VSD-Operated Patients

Start date: September 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether oral sildenafil citrate reduces the abnormal right ventricular pressure response during exercise in adolescent and adult patients with specific types of congenital heart defects.

NCT ID: NCT00762333 Recruiting - Clinical trials for Myocardial Infarction

Circulating Markers for Ischemic Heart Disease

Start date: June 2007
Phase:
Study type: Observational

The purpose of this research is to determine if two proteins in the blood are increased during acute myocardial infarction and whether their levels are higher in those who develop heart failure than those who do not. These two proteins are produced and potentially released when the heart muscle is damaged. They may then be released into the blood and be detected by standard method in the research laboratory. At this time, detection of an increase in these proteins in the blood is not known to be associated with any disease or myocardial infarction.

NCT ID: NCT00745628 Recruiting - Clinical trials for Coronary Heart Diseases

Chinese Cohort Study of Coronary Heart Disease

CCS-CHD
Start date: May 2008
Phase: N/A
Study type: Observational

Construction of coronary heart disease cohort of more than 10000 patients in China. Investigation on current situation of secondary prevention of CHD will be carried out and the effect of physician training and patient education will be evaluated.

NCT ID: NCT00741416 Recruiting - Healthy Clinical Trials

Biorepository: Indiana Health Study

IHS
Start date: June 2008
Phase: N/A
Study type: Observational

Blood samples and health information (e.g., age at diagnosis, test results) are collected for the purposes of genetic research. The blood samples are assigned a number and stored in a repository for safe keeping until they are needed for a research project. Participants are persons who are healthy (not having high blood pressure, diabetes, or high cholesterol levels) or persons who have Coronary Artery Disease (CAD) and live in Indiana. Participants complete a questionnaire at the time the blood sample is drawn and are contacted once a year to update their health history. Researchers apply to the Fairbanks Institute for use of the blood samples and health information minus participant names and contact information. Their research is required to be related to find genes or substances made by genes that may be involved in Coronary Artery Disease with the purpose of improving the investigators understanding of the illness potentially leading to the development of new diagnostic tools for identifying the illness, new treatments,or preventative measures. This study will be repeated for other disorders like Diabetes and Cancer.