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Coronary Arteriosclerosis clinical trials

View clinical trials related to Coronary Arteriosclerosis.

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NCT ID: NCT00240318 Completed - Clinical trials for Coronary Arteriosclerosis

A Study To Evaluate the Effect of Rosuvastatin On Intravascular Ultrasound-Derived Coronary Atheroma Burden (ASTEROID)

Start date: November 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see if 40 mg of rosuvastatin taken daily will reduce the atherosclerosis (fatty deposits) in your arteries

NCT ID: NCT00238004 Active, not recruiting - Clinical trials for Coronary Arteriosclerosis

The Low HDL On Six Weeks Statin Therapy (LOW) Study

Start date: November 2005
Phase: Phase 4
Study type: Interventional

Abnormal blood cholesterol levels increase the risk of developing, or dying from heart disease. It is well recognised that if "harmful" LDL cholesterol is high, and "protective" HDL cholesterol is low, this risk is increased. Drugs called statins are routinely used in patients with heart disease, are well tolerated, and decrease the harmful LDL cholesterol levels. However, statins only increase protective HDL cholesterol to a small extent. Some patients may thus benefit from additional medication to increase protective HDL-cholesterol further. One of the most effective drugs which can do this is nicotinic acid. This drug is well established having been available for over 30 years. Previous use has been limited by facial flushing in a large percentage of patients receiving the drug. However a new formulation called Niaspan is now available which is associated with much less flushing. Although many patients will have transient flushing, it is estimated that only 1 patient out of every 20 receiving the drug will have to discontinue treatment. We therefore propose, in patients with coronary artery disease and low HDL cholesterol despite being on a statin, to study the effect of Niaspan on HDL cholesterol and other lipid parameters, and to assess its tolerability.

NCT ID: NCT00235846 Completed - Clinical trials for Coronary Arteriosclerosis

Endoscopic Vessel Harvesting During Coronary Bypass Surgery

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

Conventional open vein harvesting from the legs during coronary artery bypass surgery result in wound complications among 30% of the patients. Endoscopic harvesting decrease the complication rate, but it remains to be shown whether this is also a fact among patient in whom only short segments of veingraft material is needed from the leg. We hypothesise that the rate of wound complications will be reduced and the patient satisfaction will be increased also among patients in whom only short vein segments are endoscopically harvested compared to conventional open vein harvesting.

NCT ID: NCT00213746 Completed - Clinical trials for Myocardial Infarction

Evaluation of Myocardial Viability by Means of Low-dose Dobutamine Gated SPECT (the DOGS Study)

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

Viability assessment remains a clinical challenge in patient with coronary artery disease and left ventricular dysfunction. Several imaging modalities are available for evaluating myocardial viability, based either on perfusion or on contractile reserve analysis. Briefly, perfusion analysis is highly sensitive and contractile reserve highly specific. A combined analysis of both perfusion and contractile reserve has been proposed to improve the diagnostic accuracy in patient referred for a revascularization procedure. However, the value of this combined analysis has not been validated in unselected patients referred for viability assessment. The patients enrolled in the study will undergo a nitrate enhanced rest gated SPECT using a Tc-99m labeled tracer (sestamibi or tetrofosmine) followed by a second gated SPECT acquired during a low-dose dobutamine infusion (10 mcg/kg/mn). All patients will have a 6-month clinical and imaging follow-up, including physical examination and a nitrate enhanced rest gated SPECT using the same radiopharmaceutical. All treatments received during this 6-month period will be recorded, including medical therapy and coronary revascularization (angioplasty, stenting and CABG). Finally, the value of baseline perfusion and contractile reserve analysis in predicting left ventricular ejection fraction changes at 6-month follow-up will be evaluated.

NCT ID: NCT00172536 Completed - Clinical trials for Coronary Arteriosclerosis

Effects of Exercise Training on Left Ventricular Function in Type 2 Diabetic Patients Post Coronary Artery Bypass Graft

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

The purpose of this study is to investigate the changes of cardiorespiratory fitness and left ventricular function in type 2 diabetes after uncomplicated coronary artery bypass graft (CABG) surgery. We hypothesize that exercise capacity, left ventricular diastolic function, and biochemical data improves after 12-wk exercise training in patients with type 2 diabetes underwent CABG.

NCT ID: NCT00163202 Completed - Clinical trials for Hypercholesterolemia

Comparative Atorvastatin Pleiotropic Effects

CAP
Start date: June 2002
Phase: Phase 4
Study type: Interventional

The primary objective of the study is to evaluate the efficacy of atorvastatin 80 mg daily as compared to atorvastatin 10 mg daily in reducing C-reactive protein levels over a 26-week treatment period in subjects with documented coronary artery disease.

NCT ID: NCT00159991 Active, not recruiting - Clinical trials for Ischemic Heart Disease

Copenhagen Arterial Revascularization Randomized Patency and Outcome Trial

CARRPO
Start date: February 2002
Phase: Phase 3
Study type: Interventional

There is a remarkable lack of randomized trials concerning the potential benefit of using arterial conduits for coronary bypass surgery. This is the purpose of the present trial. Exclusive use of arterial conduits might result in improved conduit viability, reduced risk of recurrent angina, myocardial infarction and other cardiac events, reduced need for antianginal medication, improved functional status and possibly improved long term survival. The patients will be followed for ten years after surgery.

NCT ID: NCT00159926 Terminated - Clinical trials for Coronary Arteriosclerosis

Cleansing of Suction Blood in Cardiac Surgery for Reduced Inflammatory Response

Start date: January 2003
Phase: Phase 3
Study type: Interventional

Cardiac surgery using heart and lung machine produces an inflammatory reaction in the body. This leads in few percent of cases to heart, lung, and kidney disturbances that potentially causes death. White blood cells in contact with the heart and lung machine and external surfaces release mediators partly responsible for this. Blood collected by the suction and the blood remaining in the heart and lung machine after its use, can be cleaned by a cell saver before reinfusion, and this might reduce the inflammatory response.

NCT ID: NCT00155012 Recruiting - Clinical trials for Coronary Arteriosclerosis

Clinical Application of MDCT in Coronary Artery Disease

Start date: August 2004
Phase: Phase 3
Study type: Observational

1) Establish normal value for coronary calcium scoring in Taiwan. 2) Find out the relationship of coronary calcium deposition and coronary artery stenosis. Propose a clinical management guideline based on coronary calcium score. 3) Evaluate sensitivity/specificity of coronary CT angiography and the influence of coronary calcium score on coronary CT angiography. 4) Evaluate the clinical application of myocardial enhancement measurement.

NCT ID: NCT00139399 Completed - Clinical trials for Coronary Arteriosclerosis

Radial Artery Versus Saphenous Vein Patency (RSVP) Study

RSVP
Start date: May 1998
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the radial artery (artery in the arm) or saphenous vein (vein in the leg), when used as bypass grafts for coronary artery bypass surgery, have a greater patency rate (degree of opening)at 5 years after surgery.