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Heart Disease clinical trials

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NCT ID: NCT00081913 Completed - Myocardial Ischemia Clinical Trials

Stem Cell Study for Patients With Heart Disease

Start date: January 2004
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if cell therapy with your own cells (autologous cells) delivered with a catheter to regions of the heart with poor blood flow will be safe and if it will relieve your chest pain and/or your ability to exercise.

NCT ID: NCT00067249 Completed - Depression Clinical Trials

Women's Use of Alternative Medicine: A Multiethnic Study

Start date: April 2001
Phase: N/A
Study type: Observational

The purpose of this study is to examine socio-cultural factors of women’s use of complementary and alternative medicine (CAM). The effects of socioeconomic status, social networks and acculturation on CAM use will be assessed among white, African-, Mexican-, and Chinese-American women.

NCT ID: NCT00041938 Completed - Stroke Clinical Trials

Warfarin Versus Aspirin in Reduced Cardiac Ejection Fraction (WARCEF) Trial

WARCEF
Start date: October 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine which of two treatments, Warfarin or aspirin, is better for preventing death and stroke in patients with poor heart function. We are now transitioning into the sub-analysis part of the WARCEF patient data. The study has recently completed data analysis for its Primary Aim. All randomized patients have completed their follow up. All study related procedure as per the protocol has been completed. We are now in the extension phase of the study to obtain more patient data to address further aims of the study. No new procedures are performed and data already in place at the sites will be collected (EKG and echocardiograms). The aims for this study extension are: - To assess progression of cardiac dysfunction over time among heart failure patients - To correlate prognosis with cardiac dysfunction

NCT ID: NCT00013949 Completed - Heart Disease Clinical Trials

Cardiovascular Vulnerability to Particulate Exposure

Start date: September 1998
Phase: N/A
Study type: Observational

This project is part of a program project directed toward assessing cardiac effects of particulate and other ambient air pollutants. In this project active elderly adults living in the communities of Boston and Steubenville have attended 12 weekly sessions including approximately 40 minutes of Holter monitoring, blood pressure, and oximetry evaluation before, during, and after outdoor exercise. To investigate the relation of air pollution to cardiac and pulmonary rehabilitation, a second portion of this study involves abstraction of blood pressure and symptom data and downloading of available repeated measures telemetry data in two populations. These populations include: 1) 200 outpatients attending 8 to 36 repeated weekly exercise training sessions in a major hospital cardiac rehabilitation unit.

NCT ID: NCT00012493 Completed - Heart Disease Clinical Trials

Cardiac Vulnerability in Potentially Susceptible Patients

Start date: October 1999
Phase: N/A
Study type: Observational

This project is part of a program project directed toward assessing cardiac effects of particulate and other ambient air pollutants. In this project patient who have recently suffered a cardiac event are being monitored with cardiac monitors for 24 hours up to 4 times during the year following their cardiac event. Similarly a second group of patients with moderate to severe heart failure will undergo similar cardiac monitoring for 24 hours, twice a week separated by 3 months. In both sets of patients home indoor pollution measures will be continuously made and used to correlate with measures of heart rate variability.

NCT ID: NCT00001746 Completed - Heart Disease Clinical Trials

Screening for Inherited Heart Disease

Start date: April 1998
Phase: N/A
Study type: Observational

Genetically inherited heart diseases like hypertrophic cardiomyopathy (HCM) are conditions affecting the heart passed on to family members by abnormalities in genetic information. These conditions are responsible for many heart related deaths and illnesses. Presently, there are several research studies being conducted in order to improve the understanding of disease processes and symptoms associated with genetically inherited heart diseases. This study is designed to determine the eligibility of patients diagnosed with or suspected to have inherited heart disease to participate in these research studies.

NCT ID: NCT00001638 Completed - Heart Disease Clinical Trials

Magnetic Resonance Imaging of the Blood Vessels of the Heart

Start date: September 29, 1997
Phase:
Study type: Observational

This study is directed at evaluating patients with "myocardial ischemia" or poor blood supply to the heart muscle due to coronary artery disease. The major objective of this study is to determine the level of safety and effectiveness of magnetic resonance imaging at diagnosing coronary artery disease. In addition, this study will allow researchers at the National Institutes of Health to see a broad spectrum of disease, preserve clinical skills, and stimulate future ideas for clinical research....

NCT ID: NCT00001460 Completed - Arrhythmia Clinical Trials

Evaluation and Treatment of Heart Disease in Patients Not Participating in Research

Start date: January 1995
Phase: N/A
Study type: Interventional

There is an important need to maintain clinical skills, provide quality training and expertise, and provide an environment that stimulates ideas for clinical research. This study permits inpatient evaluation and management of patients with heart disease who do not qualify to participate in studies currently being conducted by the Cardiology Branch of the National Heart, Lung, and Blood Institute.

NCT ID: NCT00001400 Completed - Heart Disease Clinical Trials

Outpatient Evaluation of Patients With Known or Suspected Heart Disease

Start date: December 1993
Phase: N/A
Study type: Observational

This study is designed to screen patients with heart diseases who may qualify to participate in other research studies being conducted by the Cardiology Branch of the National Heart, Lung, and Blood Institute (NHLBI). Patients participating in this research study will be seen on an outpatient basis and undergo a general medical evaluation, including blood tests, urine, examination, chest x-ray and electrocardiogram (EKG). In addition, patients may be asked to have an echocardiogram (ultrasound scan of the heart) and to perform an exercise stress test. Patients participating in this study will not receive any investigational treatments.

NCT ID: NCT00001203 Completed - Diabetes Mellitus Clinical Trials

Deferoxamine for the Treatment of Hemochromatosis

Start date: April 22, 1985
Phase:
Study type: Observational

When patients receive repeated blood transfusions the level of iron in the patient s blood can rise. When iron is processed in the body a protein known as hemosiderin can begin collecting in the organs. If too much hemosiderin collects in the organs they can begin to malfunction. This condition is called transfusional hemochromatosis. An organ of particular importance in transfusional hemochromatosis is the heart. Patients born with diseases requiring blood transfusions at birth begin to develop heart problems in their teens. These patients typically only live for 17 years. Adults that require transfusions can begin experiencing heart problems after 100-200 units of backed red blood cells. Deferoxamine (Desferal) is a drug that binds to iron and allows it to be excreted from the body. It is the only effective way to remove iron from patients who have been overloaded with iron because of multiple transfusions. Previous studies have lead researchers to believe that deferoxamine, when given as an injection under the skin (subcutaneous), can be delay or prevent heart complications. Researchers plan to continue studying patients receiving deferoxamine as treatment for the prevention of heart complications associated with repeated blood transfusions. In this study researchers will attempt; 1. To determine if deferoxamine, given regularly, can indefinitely prevent the heart, liver, and endocrine complications associated with transfusional hemochromatosis 2. To determine whether heart disease caused by transfusional hemochromatosis can be reversed by intensive treatment with deferoxamine.