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Acute Coronary Syndromes clinical trials

View clinical trials related to Acute Coronary Syndromes.

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NCT ID: NCT00665834 Completed - Dyslipidemia Clinical Trials

Comparison of Rosuvastatin and Atorvastatin in Patients With Acute Coronary Syndrome

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

This is a 3-month, randomized, parallel-group study with 2 periods, comparing the efficacy and the safety of rosuvastatin 20 mg versus atorvastatin 80 mg in patients with an acute coronary syndrome (ACS).

NCT ID: NCT00627809 Completed - Clinical trials for Acute Myocardial Infarction

Effect of Adjunctive Intracoronary Streptokinase on Late Term Left Ventricular Infarct Size and Volumes in Patients With Acute Myocardial Infarction

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

The investigators hypothesized that complementary intracoronary streptokinase administration to primary percutaneous intervention in patients with acute myocardial infarction may provide limitation infarct size and improvement in left ventricular volumes and function in acute and late phases (6 months).

NCT ID: NCT00494247 Completed - Clinical trials for Coronary Heart Disease

Endothelial Progenitor Cells-capture Stents in Acute Coronary Syndromes

JACK-EPC
Start date: October 2007
Phase: Phase 4
Study type: Interventional

Randomized prospective study to compare the efficiency and safety of EPC-capture stents (Genous, OrbusNeich) and bare metal stents with concommitant high dose atorvastatin in reduction of neointimal formation assessed by quantitative coronary angiography and IVUS. Also the association between the function (transcriptional activity, migration) and number of circulating EPCs and angiographic outcomes will be investigated.

NCT ID: NCT00464087 Completed - Clinical trials for Acute Coronary Syndromes

Switching From Fondaparinux to Bivalirudin or Unfractionated Heparin in ACS Patients Undergoing PCI

SWITCHIII
Start date: June 2007
Phase: Phase 3
Study type: Interventional

The primary objective of this clinical trial is to evaluate safety of switching from fondaparinux to either unfractionated heparin or bivalirudin for patients experiencing acute coronary syndrome undergoing percutaneous coronary angioplasty.

NCT ID: NCT00430820 Completed - Clinical trials for Coronary Artery Disease

Discovery of New Circulating Biomarkers of Coronary Atherosclerosis

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

The study hypothesis is that differential proteomic techniques can be used to discover new circulating biomarkers of coronary atherosclerosis in the blood of patients suffering from coronary artery disease (either stable or unstable) who will be compared to a group of patients without coronary artery disease

NCT ID: NCT00405717 Completed - Clinical trials for Ischemic Heart Disease

Effects of Atorvastatin Versus Pravastatin on Platelet Inhibition by Clopidogrel

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

Clopidogrel and statins are frequently coadministered in patients with ischemic heart diseases. Recent reports suggested that clopidogrel's effectiveness in inhibiting adenosine diphosphate (ADP)-induced platelets aggregation is attenuated by co-administration of certain statins. The objective of the present study is to define which kind of statins might interfere with the antiaggregation property of clopidogrel in patients with acute coronary Syndrome after percutaneous coronary intervention (PCI). In this prospective randomized study, all patients in test group will receive clopidogrel plus atorvastatin, and all patients in control group will receive clopidogrel plus pravastatin. All patients will be followed up for one year. The primary endpoints include death, non fatal AMI, urgent revascularization. The secondary endpoints include hemorrhage events and subacute thrombosis events at 1 year.

NCT ID: NCT00404781 Completed - Clinical trials for Ischemic Heart Disease

Effects of Optimized Antiplatelet Treatment After Percutaneous Coronary Intervention

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

Effects of dual antiplatelet therapy with aspirin and clopidogrel after percutaneous coronary intervention has been proven. However, patients with low response to those agents are reported be associated with adverse clinical outcomes. We suppose that optimized antiplatelet therapy for individual patients based on platelet function assay may improve long-term outcomes especially in patients with high risk of thrombosis. In this prospective randomized study, patients in control group all receive standard dual antiplatelet therapy, and patients in optimized group receive different antiplatelet therapy according to risk stratification.

NCT ID: NCT00225719 Completed - Clinical trials for Acute Coronary Syndromes

Effect of rHDL on Atherosclerosis - Safety and Efficacy: THE ERASE TRIAL

Start date: July 2005
Phase: Phase 2
Study type: Interventional

Currently available therapies to treat Acute Coronary Syndromes(ACS) have several limitations including; the relatively long treatment duration required before apparent significant benefit; the inability to achieve reversal of the atherosclerotic process; and poor patient compliance due to chronicity of therapy. This study will assess the effects of rHDL compared with placebo on indices of atherosclerosis progression and regression as assessed with intravascular ultrasound (IVUS) in patients after acute coronary syndromes (ACS).

NCT ID: NCT00214630 Completed - Clinical trials for Acute Coronary Syndromes

LUNAR IIIb Study Comparing Rosuvastatin and Atorvastatin in Subjects With Acute Coronary Syndromes

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

Comparison of rosuvastatin and atorvastatin in subjects with acute coronary syndromes

NCT ID: NCT00097591 Completed - Clinical trials for Coronary Arteriosclerosis

A Comparison of Prasugrel (CS-747) and Clopidogrel in Acute Coronary Syndrome Subjects Who Are to Undergo Percutaneous Coronary Intervention

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

The sponsors of this investigational drug are developing prasugrel (also known as CS-747) as a possible treatment for patients with acute coronary syndrome (heart attack or chest pain) who need, or are expected to need, a percutaneous coronary intervention (PCI; also called a balloon angioplasty). Prasugrel was compared with Clopidogrel to determine which drug is better at reducing deaths, future heart attacks, or stroke.