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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT00088179 Completed - Clinical trials for Coronary Artery Disease

Pexelizumab in Patients Undergoing Coronary Artery Bypass Grafting With Cardiopulmonary Bypass (PRIMO-CABG II)

Start date: July 2004
Phase: Phase 3
Study type: Interventional

During a heart bypass procedure, a substance called "complement" is activated by the body. This "complement activation" causes an inflammatory response that can lead to side affects such as chest pain, heart attacks, stroke, heart failure, or death. The purpose of this study is to find out if the study drug (pexelizumab), that blocks "complement activation," can reduce such side effects and be given safely to patients requiring the bypass procedure with the use of the heart-lung machine.

NCT ID: NCT00087893 Completed - Clinical trials for Cardiovascular Diseases

Epidemiology of Vascular Inflammation & Atherosclerosis

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

To investigate the relationship of vascular cell phenotypes to atherosclerosis.

NCT ID: NCT00086450 Active, not recruiting - Clinical trials for Cardiovascular Diseases

Comparison of Two Treatments for Multivessel Coronary Artery Disease in Individuals With Diabetes (FREEDOM)

Start date: April 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare 5-year mortality rates in diabetic individuals with multivessel coronary artery disease (CAD) who undergo either coronary artery bypass grafting (CABG) surgery or percutaneous coronary stenting.

NCT ID: NCT00086424 Completed - Heart Failure Clinical Trials

Epidemiology of Insulin Growth Factor (IGF) and Cardiovascular Events

Start date: July 2004
Phase:
Study type: Observational

To explore the role of insulin growth factor in cardiovascular disease in older men and women.

NCT ID: NCT00083824 Completed - Clinical trials for Cardiovascular Diseases

Estrogen, HDL, and Coronary Heart Disease in Women

Start date: March 2004
Phase: Phase 2/Phase 3
Study type: Interventional

To clarify the effects of estrogen, with or without progestin, on high density lipoprotein (HDL) in postmenopausal women.

NCT ID: NCT00082121 Completed - Myocardial Ischemia Clinical Trials

Safety and Efficacy of TP10, a Complement Inhibitor, in Adult Women Undergoing Cardiopulmonary Bypass Surgery

Start date: April 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if the study drug (TP10), which blocks complement release, can reduce such side effects of complement inflammation as chest pain or heart attacks and be taken safely in women who undergo cardiopulmonary bypass surgery.

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: NCT00081705 Completed - Clinical trials for Cardiovascular Diseases

Estrogen Receptor Variants, HDL, and Atherosclerosis

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

To measure the association between estrogen receptor variants and the extent of atherosclerosis in the thoracic and abdominal aorta and the right coronary artery in subjects in the PDAY study.

NCT ID: NCT00081666 Completed - Clinical trials for Cardiovascular Diseases

Logical Analysis of Data and Cardiac Surgery Risk

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

To use a new statistical method, the Logical Analysis of Data (LAD), to predict cardiac surgery risk.

NCT ID: NCT00080587 Completed - Coronary Disease Clinical Trials

Atherosclerosis in the Coronary and Carotid Arteries

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

This study will compare changes in atherosclerotic plaque in the coronary arteries (vessels on the surface of the heart that supply blood to the heart) with changes in the carotid arteries (vessels in the neck that supply blood to the brain) in patients enrolled in a Pfizer-sponsored treatment trial for coronary artery disease. Atherosclerosis is a buildup of fatty deposits (plaque) in arteries that can lead to blockage of the vessel, possibly resulting in heart attack or stroke. A major question in cardiovascular disease is how closely atherosclerotic changes in the coronary arteries correlate with changes in the carotid artery that occur with treatment. substudy of a Pfizer. Patients enrolled in the Pfizer trial comparing the effectiveness of the drug atorvastatin with a combination of atorvastatin and CETP inhibitor (a drug to increase HDL cholesterol levels) may be eligible for this substudy. Participants undergo magnetic resonance imaging (MRI) and ultrasound of the carotid arteries to measure the thickness of the vessels. The results are then compared with the coronary artery images obtained as part of the patient's evaluation for the Pfizer trial. MRI MRI scans use a powerful magnet with an advanced computer system and radio waves to produce accurate, detailed pictures of organs and tissues. During the scan the patient lies on a table in a narrow cylinder containing a magnetic field, wearing earplugs to muffle loud noises that occur with electrical switching of the magnetic fields. A medicine called gadolinium contrast may be injected into a vein during part of the scan to brighten the images. The scan takes about 30 to 90 minutes. An electrocardiogram (ECG) is done during the scan to monitor the heart's electrical activity. Patients who agree to undergo another MRI test are also imaged in a scanner that uses a stronger (3 Tesla) magnet. Ultrasound An echocardiogram (ultrasound of the heart) uses sound waves to image the carotid arteries. A gel is applied to the area of the neck to be imaged and a small handheld ultrasound probe is held against the neck to take the pictures. Participants return after 2 years for a second set of tests.