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Heart Disease clinical trials

View clinical trials related to Heart Disease.

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NCT ID: NCT00500929 Completed - Heart Disease Clinical Trials

A Clinical Trial in Higher Risk Geriatric Patients Undergoing OHSP

MiniMetrxics
Start date: July 2007
Phase: Phase 2
Study type: Interventional

To provide information on parameters needed to design a subsequent Phase III confirmatory trial and to assess the safety and efficacy of the acute use of CMI X-11S in high-risk geriatric patients undergoing open-heart surgical procedures (OHSP) requiring cardio-pulmonary bypass.

NCT ID: NCT00420160 Completed - Lung Cancer Clinical Trials

Does Moderate Intensity Exercise Help Prevent Smoking Relapse Among Women?

Start date: February 2007
Phase: Phase 2/Phase 3
Study type: Interventional

This study compares the effects of a standard smoking cessation treatment, including one-time brief counseling and provision of nicotine patch plus an 8-week moderate intensity exercise program versus the same standard smoking cessation treatment plus equivalent contact control among 60 healthy women. We hypothesize that participants in the smoking cessation plus moderate intensity exercise condition will be more likely to quit smoking than participants in the smoking cessation treament plus contact control condition.

NCT ID: NCT00395148 Completed - Diabetes Clinical Trials

Improving Metabolism With HDL Cholesterol

Start date: March 2006
Phase: N/A
Study type: Interventional

High levels of good cholesterol (HDL) in our blood decreases our chance of having a heart attack. This relates in part to the role good cholesterol plays in reducing build up of fat in the arteries. However, good cholesterol has many other protective effects. We have recently identified three enzymes (proteins) activated by HDL in cells lining the blood vessels, which may be responsible for some of HDL's protective actions.

NCT ID: NCT00374361 Completed - Stroke Clinical Trials

Study of the Relationship Between Blood Vessels and Insulin Response in Adolescents

Start date: July 2003
Phase: N/A
Study type: Observational

This study is designed to determine whether there is a relationship between the way insulin and blood vessels work. The difference in the interaction between Caucasian and African American adolescents will also be examined. This may play a role in the differing rates of heart disease and diabetes between the two groups.

NCT ID: NCT00342992 Completed - Stroke Clinical Trials

Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC) Study

Start date: March 3, 1995
Phase:
Study type: Observational

The project is a passive follow-up of the Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC) Study cohort. Originally, this was a large, randomized, double-blind, placebo-controlled, 2x2 factorial primary prevention trial testing the effects of alpha-tocopherol and beta-carotene supplementation on cancer incidence and mortality. The study was conducted in Finland as a collaboration between the U.S. National Cancer Institute (NCI) and the National Public Health Institute of Finland. NCI has maintained passive surveillance of the cohort through Finnish national registries, including the cancer registry. The primary purpose of the ATBC cohort follow-up is to use the existing risk factor data and biological specimens (i.e., serum, whole blood, DNA, red blood cells, and toenails) to test hypotheses relevant to cancer etiology, survival, early detection, and prevention. These data and biospecimens continue to provide an invaluable resource for the study of biochemical, nutritional, genetic, and molecular hypotheses. These analyses are made all the more informative and powerful by the addition of cases identified annually during the follow-up period, and the research benefits from a longer pre-diagnosis period (now over 30 years).

NCT ID: NCT00296985 Completed - Heart Disease Clinical Trials

Continuous Cellsaver and Neurocognitive Decline Post Cardiac Surgery

Start date: December 2001
Phase: Phase 4
Study type: Interventional

Patients having cardiac surgery to correct their heart disease may suffer a decline in mental and neurologic abilities. Passage of small particles of fat, tissue waste and air bubbles to the brain while on the heart-lung machine is thought to be one cause for decline in mental and neurologic abilities (the function of brain) after surgery. The purpose of this study is to determine if replacement of cardiotomy suction (one part of the heart-lung machine) with the cell-saver (a different part of the heart-lung machine) during surgery will help to prevent a decline in mental and neurologic abilities after surgery. investigating 312 patients over 2 years,patients will be assigned randomly to either cardiotomy suction or cell-saver group. Patients will be given questionnaires before surgery, 6 weeks and 1-year after surgery. These questionnaires will assess memory, attention span, the ability to concentrate and the quality of life. Patients will also have a brief neurologic exam (physical examination to check mental state, reflexes, strength, and balance) before surgery, 3-5 days after surgery, 6 weeks and 1-year after surgery to determine any changes. Cell-saver separates red blood cells from tissue waste products and fat prior to returning blood back to the patient and may reduce the negative effects of particles of fat, tissue waste and air bubbles have on the brain. Potential benefits of cell-saver device when used during surgery may prevent the decrease in memory, attention span, and the ability to concentrate resulting in improved quality of life after surgery. Objectives: The primary aim is to determine the effect of continuous flow cell-saver on short and long term neurocognitive function after cardiac surgery, measured by precise preoperative and postoperative psychometric and neurologic testing. Hypothesis: The primary hypothesis: Continuous flow cell-saver reduces postoperative neurocognitive decline following cardiac surgery. Methodology: 312 informed and consenting patients, age > 65 years, scheduled for coronary artery bypass graft surgery will be prospectively enrolled over a 2-year period. Patients will be randomly allocated to either the continuous flow cell-saver or conventional cardiotomy suction (controls). Neurological history and physical exam will be completed preoperatively, discharge, 6-weeks and 1-year after surgery. Transcranial Doppler scanning will be used for intraoperative monitoring of cerebral embolic load. Transesophageal echocardiography and epiaortic scanning will be employed to account for the severity of the aortic atheroma scores. Neurocognitive testing and quality of life assessment will be conducted preoperatively , 6-weeks and 1-year after surgery. Significance: The utilization of continuous flow cell-saver may reduce the negative effects of fat particles, tissue waste and air emboli have on brain.

NCT ID: NCT00284011 Completed - Heart Disease Clinical Trials

Effect of the Dietary Supplement SAMe on Blood Homocysteine Levels

Start date: June 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the oral intake of the dietary supplement SAMe increases blood homocysteine levels in healthy human subjects.

NCT ID: NCT00282711 Completed - Clinical trials for Coronary Artery Disease

The WOMEN Study: What is the Optimal Method for Ischemia Evaluation in WomeN?

Start date: June 2004
Phase: N/A
Study type: Observational

The purpose of this study is to compare two types of exercise stress testing to find the best method for detecting heart disease in women.

NCT ID: NCT00224237 Completed - Stroke Clinical Trials

Exploring Folk Health Practices in Latinos With Chronic Medical Conditions

Start date: December 2005
Phase: N/A
Study type: Observational

This study will explore how culture influences the use of folk healing practices and medical services in Latinos with chronic medical conditions.

NCT ID: NCT00205387 Completed - Heart Disease Clinical Trials

Cardiac Elastography to Determine Strain and Strain Rates in the Heart

Start date: November 2005
Phase: N/A
Study type: Observational

Cardiac elastography is a new technique to analyze strain and strain rates in many organ systems, including the heart. In this study, cardiac elastography derived from the analysis of raw radiofrequency data obtained from a conventional clinical echocardiograph system will be compared to processed information that comes from the same echocardiograph system. The purpose of this study is to determine if cardiac elastography can accurately determine strain and strain rates as compared to more conventional means.