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Coronary Disease clinical trials

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NCT ID: NCT00536965 Completed - Diabetes Mellitus Clinical Trials

Percentage of Secondary Prevention Patients Treated to Their LDL-C Targets

Start date: July 2007
Phase: N/A
Study type: Observational

A cholesterol/lipid profile screening project of high risk patients with hyperlipidaemia (secondary prevention) who already receive cholesterol-lowering therapy. Lipid profile and rate of patients who are treated to target (which is <100mg/dl for patients with high risk and <70mg/dl for patients at very high risk) are screened (office-based specialists). The doctors therapy decisions after the screening and possible reasons for these decisions will be documented. Our aim is to evaluate dosing habits, to evaluate how many patients are treated to their LDL-C target and to underline the importance of treating patients to their cholesterol targets.

NCT ID: NCT00536796 Completed - Diabetes Mellitus Clinical Trials

Percentage of Secondary Prevention Patients Treated to Their LDL-C Targets

Start date: September 2007
Phase: N/A
Study type: Observational

A cholesterol/lipid profile screening project of high risk patients with hyperlipidaemia (secondary prevention) who already receive cholesterol-lowering therapy. Lipid profile and rate of patients who are treated to target (which is <100mg/dl for patients with high risk and <70mg/dl for patients at very high risk) are screened (hospital-based specialists). The doctors therapy decisions after the screening and possible reasons for these decisions will be documented. Our aim is to evaluate dosing habits, to evaluate how many patients are treated to their LDL-C target and to underline the importance of treating patients to their cholesterol targets.

NCT ID: NCT00535405 Completed - Clinical trials for Hypercholesterolemia

A Study to Assess the Cholesterol Lowering Effect of Ezetimibe/Simvastatin Combination Tablet Compared to Another Cholesterol Lowering Drug in Elderly Patients With High Cholesterol at High or Moderately High Risk for Coronary Heart Disease (0653A-128)

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

A multicenter study to evaluate the safety and efficacy of ezetimibe/simvastatin versus atorvastatin in elderly patients with high cholesterol at high or moderately high risk for coronary heart disease.

NCT ID: NCT00534651 Completed - Clinical trials for Coronary Arteriosclerosis

Paracetamol and Endothelial Function in Patients With Stable Coronary Artery Disease

Start date: November 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of orally given paracetamol on the vascular function and on 24-hour blood pressure in patients with coronary artery disease

NCT ID: NCT00533039 Completed - Clinical trials for Coronary Artery Disease

sPLA2 Inhibition to Decrease Enzyme Release After PCI Trial

SPIDER-PCI
Start date: October 2007
Phase: Phase 2
Study type: Interventional

As evidence accumulates that atherogenesis or Coronary Artery Disease (CAD) may not be simply a disorder of lipid metabolism, but an inflammatory disease, the focus of treatment has shifted. A-002 or Varespladib is an anti-inflammatory drug for treatment of chronic and acute diseases. It acts by inhibiting secretory phospholipase A2 (sPLA2 ) - one of a family of enzymes leading to inflammation - which may be important in: 1) the development of atherosclerosis and 2) the increase in occurence of cardiovascular events after angioplasty. Previous studies have demonstrated that sPLA2: 1) facilitates the pro-atherogenic effects of low-density (LDL or bad cholesterol) and 2) increased levels post-angioplasty correlate with an increased risk of events at followup contact. Therefore this study proposes to investigate the ability of A-002 to prevent or reduce myocardial damage after angioplasty by inhibiting the cascade of inflammatory mediators. Substudy - Subjects who agree will also have a vascular ultrasound 24h post-PCI to assess endothelial function.

NCT ID: NCT00531011 Completed - Clinical trials for Coronary Artery Disease

EXecutive RCT: Evaluating XIENCE V® in a Multi Vessel Disease

EXecutive
Start date: September 2007
Phase: Phase 4
Study type: Interventional

The purpose of this two part study is the assessment of the performance of the XIENCE V® Everolimus Eluting Coronary Stent System (XIENCE V® EECSS) in the treatment of the specific setting of patients with Multi-Vessel Coronary Artery Disease (MVD).

NCT ID: NCT00528515 Completed - Clinical trials for Coronary Artery Disease

Desflurane Versus Propofol Anesthesia for Off-Pump CABG

Start date: February 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to prove if anesthesia maintained with the inhaled volatile anesthetic desflurane is superior to the intravenously applied propofol anesthesia in off-pump coronary artery bypass grafting (OP-CABG) surgery as measured by following parameters: 1. hemodynamic parameters during and after the operation, 2. pulmonary gas exchange, need for mechanical ventilation and for ICU and intrahospital stay, 3. release of heart muscle injury markers in response to surgery and intraoperative ischaemia, 4. inflammatory response to the operation. We suspect that insufflation anesthesia with desflurane may be superior to intravenous anesthesia with propofol.

NCT ID: NCT00528411 Completed - Clinical trials for Coronary Artery Disease

A Study of the Onset and Offset of Antiplatelet Effects Comparing Ticagrelor, Clopidogrel, and Placebo With Aspirin

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

The purpose of this study is to see how Ticagrelor, a new oral reversible anti-platelet medication, affects platelets. Anti-platelet agents are medications that block the formation of blood clots by preventing the clumping of platelets. Blood clots prevent us from bleeding, but when they form inside the arteries their formation is linked to a risk of medical problems such as heart attack and stroke. This study investigated how long it takes for Ticagrelor to begin working and how long it takes for it to stop working after the last dose of drug. Ticagrelor will be compared to clopidogrel, an established anti-platelet treatment for preventing blood clots, and placebo plus Aspirin.

NCT ID: NCT00525954 Completed - Clinical trials for Coronary Artery Disease

PLASMA 2 Trial: Examination of Once Daily (QD) Dosing of A-002 In Subjects With Stable Coronary Artery Disease

PLASMA 2
Start date: September 2007
Phase: Phase 2
Study type: Interventional

The study will be conducted at up to 25 U.S. centers and will be a double-blind randomized parallel group placebo controlled study among subjects with stable coronary artery disease (CAD). Subjects will be randomized to receive either placebo tablets or one of 2 orally active doses of A-002. The duration of study drug therapy will be 8 weeks.

NCT ID: NCT00525824 Completed - Atherosclerosis Clinical Trials

12-week Open-label, Phase IIIb Comparing Efficacy and Safety of Rosuvastatin (CRESTORâ„¢) in Combination With Ezetimibe

GRAVITY
Start date: August 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether treatment of Rosuvastatin (CRESTORâ„¢) or Simvastatin given as monotherapy or given in combination with Ezetimibe, will lower the Low Density Lipoprotein Cholesterol (LDL-C) in patients with Hypercholesterolaemia and Coronary Heart Disease (CHD) or a CHD Risk Equivalent, Atherosclerosis or a 10-year CHD Risk of >20%