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Acute Coronary Syndrome clinical trials

View clinical trials related to Acute Coronary Syndrome.

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NCT ID: NCT01953276 Completed - Clinical trials for Acute Coronary Syndrome

Are Serial Electrocardiograms Additive to SeriAl Second-generations Troponins in Predicting Acute CoronAry Syndromes in PatienTs With Undifferentiated cHest Pain

ASAP Cath
Start date: January 2013
Phase:
Study type: Observational

Our research will examine whether the presence or absence of serial electrocardiogram (ECG) changes aids in reclassifying participants' risk for major adverse cardiac events (MACE) over and above serial blood testing.

NCT ID: NCT01952392 Completed - Clinical trials for Acute Coronary Syndrome

Prevention of Cardiovascular Events by Antiplatelet Agents After Acute Coronary Syndrome

AReMIS
Start date: October 2013
Phase: N/A
Study type: Observational

Prevention of cardiovascular events by antiplatelet agents after acute coronary syndrome

NCT ID: NCT01951001 Completed - Clinical trials for Acute Coronary Syndrome

Fixed-dose vs. Phenotype-based PrAsugrel Dose to MATCH Therapeutic Zone in Asians With Acute Coronary Syndrome

Start date: July 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the fixed-dose (prasugrel 10 mg/d vs. 5 mg/d) vs. phenotype (platlet function test by VerifyNow P2Y12 assay)-based prasugrel dose adjustment can match therapeutic zone of platelet reactivity in PCI-treated Asians with acute coronary syndrome

NCT ID: NCT01947998 Completed - Atrial Fibrillation Clinical Trials

Study of Rivaroxaban Use and Potential Adverse Outcomes in Routine Clinical Pratice (UK)

Start date: December 22, 2011
Phase:
Study type: Observational

This prospective cohort study will provide information about: characteristics of Rivaroxaban use in patients who are prescribed Rivaroxaban for the first time compared to patients who are prescribed Warfarin for the first time, the occurrence of intracranial haemorrhage, gastrointestinal and urogenital bleeding, and the occurrence of non-infective liver disease.

NCT ID: NCT01947985 Completed - Atrial Fibrillation Clinical Trials

Study of Rivaroxaban Use and Potential Adverse Outcomes in Routine Clinical Pratice (Netherlands)

Start date: February 1, 2012
Phase:
Study type: Observational

This prospective cohort study will provide information about: characteristics of Rivaroxaban use in patients who are prescribed Rivaroxaban for the first time compared to patients who are prescribed Acenocoumarol for the first time, the occurrence of intracranial haemorrhage, gastrointestinal and urogenital bleeding, and the occurrence of non-infective liver disease.

NCT ID: NCT01947959 Completed - Atrial Fibrillation Clinical Trials

Study of Rivaroxaban Use and Potential Adverse Outcomes in Routine Clinical Practice (Germany)

Start date: December 22, 2011
Phase:
Study type: Observational

This prospective cohort study will provide information about: characteristics of Rivaroxaban use in patients who are prescribed Rivaroxaban for the first time compared to patients who are prescribed Phenprocoumon for the first time, the occurrence of intracranial haemorrhage, gastrointestinal and urogenital bleeding, and the occurrence of non-infective liver disease.

NCT ID: NCT01944800 Completed - Clinical trials for Acute Coronary Syndrome (ACS)

Prospective, Randomized Trial of Ticagrelor Versus Prasugrel in Patients With Acute Coronary Syndrome

ISAR-REACT 5
Start date: September 15, 2013
Phase: Phase 4
Study type: Interventional

Aim of the randomized, open-label, multicenter ISAR-REACT 5 trial is to assess whether ticagrelor is superior to prasugrel in patients with acute coronary syndrome and planned invasive strategy in terms of clinical outcomes.

NCT ID: NCT01933581 Completed - Clinical trials for Acute Coronary Syndrome

A Study to Improve Cardiovascular Outcomes in High Risk PatieNts With Acute Coronary Syndrome

ICON1
Start date: October 2012
Phase: N/A
Study type: Observational

Coronary artery disease and heart attacks are the leading cause of death in the UK. Our population is ageing. The number of older patients suffering heart attacks and having angioplasty procedures to open up blocked heart arteries is increasing. After angioplasty, older patients (80 years of age or over) are at 5 times increased risk of death at one year compared to their predicted normal life expectancy. In addition, many patients present with further heart attacks, stroke and undergo repeat heart catheter test and angioplasty procedures. At present it is not clear who will or will not experience further problems in the future. The ability to predict who will and will not suffer future problems at the time of initial presentation can be helpful in providing additional treatment and close monitoring to those that are at risk of further problems. The ICON 1 study is set out to study just that. In this study, older patients will undergo a comprehensive evaluation of the cardiovascular disease burden by undergoing additional investigations. These results from each patient will be used to develop a risk score that will inform physicians of the patient's future risk of developing adverse events and provide a better understanding of how to manage older patients with coronary artery disease and also help plan future studies looking at treatment strategies that might be beneficial in improving outcomes.

NCT ID: NCT01931852 Completed - Clinical trials for Acute Coronary Syndrome

Cardiac Magnetic Resonance Imaging Strategy for the Management of Patients With Acute Chest Pain and Detectable to Elevated Troponin

CMR-IMPACT
Start date: September 2013
Phase: N/A
Study type: Interventional

The broad, long-term objective is to improve outcomes by optimizing healthcare delivery processes for patients with detectable to elevated serum troponin. This clinical trial involving emergency department (ED) patients with intermediate to high-risk chest pain and detectable to minimally elevated serum troponin within 6 hours of evaluation.

NCT ID: NCT01927640 Completed - Clinical trials for Acute Coronary Syndrome

Dexmedetomidine for Reversal of Cocaine's Effects on the Heart

Start date: February 1, 2013
Phase: Early Phase 1
Study type: Interventional

This study will use myocardial contrast echocardiography performed during a continuous intravenous infusion of Definity microbubbles (Perflutren lipid microbubbles) to determine if dexmedetomidine (an intravenous central sympatholytic drug) can reverse all the cardiovascular effects of low-dose intranasal cocaine—including vasoconstriction in the coronary microcirculation—both in cocaine-naïve and non-treatment seeking cocaine-addicted subjects.