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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT00566059 Completed - Clinical trials for Coronary Artery Disease

Computed Tomographic Angiography or Conventional Coronary Angiography in Clinical Decision Making

CARDUCCI
Start date: May 2006
Phase: N/A
Study type: Observational

Patients planned for elective conventional coronary angiography will undergo CT coronary angiography (Dual Source CT) in order to assess the correlation of stenosis detection and therapeutic advice between conventional and CT coronary angiography. We hypothesize that their is a good correlation between conventional and CT coronary angiography for stenosis detection and therapeutic advice.

NCT ID: NCT00565500 Completed - Osteoarthritis Clinical Trials

Celecoxib, Ibuprofen and the Antiplatelet Effect of Aspirin

Start date: April 2003
Phase: Phase 4
Study type: Interventional

Study design: Single center, placebo-controlled, double blind, parallel groups. To evaluate the potential interaction between aspirin and ibuprofen or celecoxib in patients with osteoarthritis (OA) and documented stable ischemic heart disease, a total of 24 patients chronically treated with aspirin will be randomly assigned to one of the 3 treatment groups: 1) celecoxib 200 mg bid; 2) ibuprofen 600 mg tid; 3) placebo.

NCT ID: NCT00564824 Completed - Coronary Disease Clinical Trials

The Impact of Caffeine on Brachial Endothelial Function in Healthy Subjects and in Patients With Ischemic Heart Disease

Start date: November 2007
Phase: Phase 3
Study type: Interventional

Prior work (Chris, M. et al, Clinical Science 2005; 109, 55-60) has demonstrated that drinking a cup of coffee (80-100 mg of caffeine) an hour before endothelium-dependent FMD (flow-mediated dilatation) of the brachial artery, effects endothelial function in healthy adults subjects. This effect might be attributed to caffeine, given that decaffeinated coffee (<2 mg of caffeine) was not associated with any change in endothelial performance. In the current study we intend to further examine the impact of caffeine on brachial endothelial function among healthy subjects & in patients with proven ischemic heart disease.

NCT ID: NCT00563901 Completed - Hypertension Clinical Trials

Analyzing How Genetics May Affect Response to High Blood Pressure Medications

Start date: September 2000
Phase: N/A
Study type: Observational

High blood pressure is one of the most common health problems in the United States. There are many medications to treat high blood pressure, but there is a large variance in how people respond to these medications. It is believed that genetic variations may contribute to the inconsistent treatment response. This study will use genetic analysis to determine whether particular genes interact with high blood pressure medications to modify the risk of certain cardiovascular diseases.

NCT ID: NCT00563238 Withdrawn - Myocardial Ischemia Clinical Trials

Beta-blocker Before Extubation

Start date: November 2007
Phase: N/A
Study type: Interventional

Silent myocardial ischemia is known to occur in the general medical intensive care unit population immediately following tracheal extubation. We believe these patients are at risk for primary cardiac events in the 4 hours immediately following extubation. Metoprolol is a selective beta-1 antagonist, with little to no beta-2 activity at low and moderate doses. The cardioprotective effects of beta blockade have been well documented in randomized controlled trials. In patients undergoing extubation, prophylactic use of intravenous metoprolol may reduce post-extubation ischemia events as well as precursors of cardiogenic pulmonary edema (atrial and ventricular wall tension). Our primary hypothesis is that prophylactic metoprolol (titrated to reduce resting heart rate by at least 10%) prior to tracheal extubation will reduce the rate of ischemia as judged by ST segment analysis.

NCT ID: NCT00562952 Completed - Clinical trials for Coronary Artery Disease

Nt-proBNP Guided Primary Prevention of CV Events in Diabetic Patients

PONTIAC
Start date: November 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Increased levels of NT-proBNP are known to increase the risk of cardiac events in diabetic patients. The other way around, patients with normal values have an excellent prognosis on short-term. We intend in our study to proof the hypothesis, whether it is possible to decrease NT-proBNP levels by intensified cardiac prevention care We aim those patients, who already have elevated levels, although no history of a cardiac disease. This decrease in NT-proBNP should be translated consequently in a decrease in cardiac events

NCT ID: NCT00562679 Completed - Clinical trials for Coronary Artery Disease

Coronary Artery Disease and Sleep Apnea

Start date: March 1992
Phase: N/A
Study type: Observational

The purpose of this study is to determine the effect of sleep apnea on mortality, stroke and myocardial infarction among 408 patients with coronary artery disease referred for evaluation of coronary intervention who were examined with overnight cardio respiratory monitoring between March 1992 and June 1995.

NCT ID: NCT00562016 Terminated - Clinical trials for Coronary Artery Disease

Protect II, A Prospective, Multicenter Randomized Controlled Trial

PROTECT II
Start date: October 2007
Phase: Phase 3
Study type: Interventional

The IMPELLA® 2.5 System will be superior to Intra Aortic Balloon Pump in preventing the composite rate of major adverse events during and after the PCI procedure.

NCT ID: NCT00561028 Completed - Clinical trials for Coronary Artery Disease

Chlamydia and Mycoplasma in Coronary Artery Disease

Start date: March 2002
Phase: N/A
Study type: Observational

To test the association between anti-Chlamydia serum titers and anti-Mycoplasma antibodies with Acute Coronary Syndromes.

NCT ID: NCT00560209 Completed - Clinical trials for Coronary Artery Disease

Study of ONO-1101 in Patients Scheduled for Coronary Angiography

Start date: November 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of ONO-1101 in patients scheduled for coronary angiography, in a double-blind, randomized, placebo-controlled, parallel group, multi-center study.