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Acute Coronary Syndrome clinical trials

View clinical trials related to Acute Coronary Syndrome.

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NCT ID: NCT00914420 Recruiting - Clinical trials for Coronary Artery Disease

Optical Coherence Tomography (OCT) Evaluation of Re-endothelization: A Comparison of the Intrepide™ Stent Versus Taxus™

OISTER
Start date: June 2009
Phase: Phase 4
Study type: Interventional

Patients presenting with ACS (Acute Coronary Syndrome) in the emergency department will be screened for clinical eligibility and asked to sign informed consent to the study. A total of 40 patients will be randomized. 20 of them will receive a Trapidil eluting stent (Intrepide™ stent), 20 will receive a Paclitaxel eluting stent (Taxus™ stent). After 90 days the patients who were treated with the INTREPIDE stent in the first lesion will be treated with the Taxus stent in the second lesion. After 90 days the patients who were treated with the Taxus stent in the first lesion will be treated with the INTREPIDE stent in the second lesion. Coronary angiography will be performed through the femoral (groin) or radial (wrist) artery with the use of standard techniques. The doctor will determine if the patient is qualified for enrolment at the end of the diagnostic coronary angiogram

NCT ID: NCT00822679 Recruiting - Clinical trials for Acute Coronary Syndrome

Eszopiclone and Inflammatory Mediators in Patients With Acute Coronary Syndrome

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

The purpose of the study is to examine the effects of Eszopiclone, a sleep aid, on inflammatory mediators and coagulability in patients with a recent myocardial infarction.

NCT ID: NCT00760786 Recruiting - Clinical trials for Acute Coronary Syndrome

Effects of Intensive Lipid Lowering and Omega-3 Fatty Acid on Composition of Coronary Atherosclerotic Plaque

Start date: July 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether intensive lipid lowering and Omega-3 fatty acid are effective in the treatment of coronary atherosclerotic plaque.

NCT ID: NCT00728013 Recruiting - Clinical trials for Acute Coronary Syndrome

China Intensive Lipid Lowering With Statins in Acute Coronary Syndrome

CHILLAS
Start date: December 2006
Phase: N/A
Study type: Interventional

In summary, the CHILLAS study will be the first multicenter study performed in a Chinese population using a patient-level analysis to compare the effects and safety of intensive statin therapy with that of moderate statin therapy. Therefore, it will determine whether "lower is better", that is, whether LDL cholesterol lowering to a level of approximately 100mg/dl provides a benefit inferior to that of LDL cholesterol lowering to a much lower level; examine the role of inflammatory markers in predicting cardiac events and response to statin therapy; and evaluate the effects of statin therapy on regression of coronary atherosclerosis using IVUS.

NCT ID: NCT00716430 Recruiting - Clinical trials for Acute Coronary Syndrome

European Quality Improvement Programme for Acute Coronary Syndromes

EQUIP-ACS
Start date: August 2007
Phase: N/A
Study type: Interventional

The main hypothesis to be tested is that the use of a quality improvement programme will lead to measurable improvements in the management of care and use of evidence based treatments for patients presenting to hospital with non-ST elevation acute coronary syndromes.

NCT ID: NCT00702936 Recruiting - Clinical trials for Myocardial Infarction

Telmisartan Versus Ramipril After Acute Coronary Syndrome

TERACS
Start date: November 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the antinflammatory and endothelial progenitor cell (EPC) mobilizing effect of Ramipril and Telmisartan in patients presenting with acute coronary syndrome

NCT ID: NCT00473863 Recruiting - Clinical trials for Acute Coronary Syndrome

Coronary Computed Tomographic Angiography in Emergency Department Chest Pain Patients at Intermediate Risk of Acute Coronary Syndrome

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

The purpose of this study is to determine whether Coronary Computed Tomographic Angiography (CCTA) will increase patient safety by decreasing the rate of missed ACS and adverse events in patients who receive standard care plus CCTA versus standard care alone. Additional goals of the study are to determine whether CCTA can safely reduce the duration of ED visits and the number and duration of hospital admissions.

NCT ID: NCT00470587 Recruiting - Clinical trials for Myocardial Infarction

Advantageous Predictors of Acute Coronary Syndromes Evaluation (APACE) Study

APACE
Start date: April 2006
Phase:
Study type: Observational

The triage of patients with suspected acute coronary syndrome in the emergency room is a time-consuming diagnostic challenge. Therefore high sensitive early markers for myocardial damage are needed for more rapidly rule out of acute myocardial infarction (AMI) - especially for the first 3 to 4 hours after onset of chest pain in AMI ("troponin-blind" period). Therefore we test the hypothesis that the use meticulous patient history and novel cardiac markers can provide a faster detection or exclusion of AMI in patients presenting with acute chest pain to the emergency department. The prospective cohort study is designed to enrol patients presenting with acute chest pain at rest within the last 12 hours to the emergency department. Several blood samples for detection of the new markers will be drawn and compared with the gold standard for the diagnosis of AMI (high-sensitivity cardiac troponin T). All patients will be contacted by telephone at 3, 12, 24 and 60 months to determine functional status, major adverse cardiac events (death, myocardial infarction, coronary artery bypass grafting, percutaneous coronary intervention), and the results of cardiac examination (stress test, coronary angiography) if performed.

NCT ID: NCT00354796 Recruiting - Atrial Fibrillation Clinical Trials

The Effect of Reduced Dose of Enoxaparin on the Outcomes of Treatment With Enoxaparin

Start date: July 2006
Phase: N/A
Study type: Observational

We hypothesize that reduced dose of enoxaparin in elderly patients will result in reduced proportion of patients with therapeutic anti Xa activity and reduced clinical efficacy.

NCT ID: NCT00339105 Recruiting - Clinical trials for Acute Coronary Syndrome

The Usefulness of HyperQ Recordings for the Early Diagnosis of Acute Coronary Syndrome in Patients Presenting With Chest Pain

Start date: June 2006
Phase: Phase 3
Study type: Observational

The purpose of the study is to assess the usefulness of high Frequency mid-QRS analysis in identifying the ischemic origin of patients presenting to the Emergency Room (ER)with Chest pain.