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Unstable Angina clinical trials

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NCT ID: NCT00809965 Completed - Clinical trials for Myocardial Infarction

An Efficacy and Safety Study for Rivaroxaban in Patients With Acute Coronary Syndrome

Start date: November 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether rivaroxaban in addition to standard care reduces the risk of the composite of cardiovascular death, myocardial infarction, or stroke in patients with a recent acute coronary syndrome compared with placebo.

NCT ID: NCT00774475 Not yet recruiting - Unstable Angina Clinical Trials

Dual Antiplatelet Therapy Tailored on the Extent of Platelet Inhibition

DANTE
Start date: November 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy (reduction of major ischemic events at 6 and 12 months of follow-up) of a tailored clopidogrel therapy in patients with UA/NSTEMI undergoing PCI with stent implantation and wiht a documented residual platelet reactivity assessed by a point of care system (VerifyNow P2Y12).

NCT ID: NCT00705458 Completed - Clinical trials for Coronary Artery Disease

Study Comparing CT Scan and Stress Test in Diagnosing Coronary Artery Disease in Patients Hospitalized for Chest Pain

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

The purpose of this study is to determine whether coronary artery CT scanning or nuclear stress testing is better at diagnosing chest pain patients with coronary artery disease to select appropriate candidates for coronary catheterization and re-vascularization.

NCT ID: NCT00552513 Completed - Clinical trials for Myocardial Infarction

Early Versus Delayed Timing of Intervention in Patients With Acute Coronary Syndromes

TIMACS
Start date: May 2005
Phase: N/A
Study type: Interventional

The timing of intervention study is a prospective, randomized, international, multicentre comparison of the relative efficacy, safety, and cost effectiveness of a management strategy of coronary angiography and intervention performed within 24 hours of randomization versus delayed coronary angiography and intervention in patients after 36 hours with acute coronary syndromes (ACS).

NCT ID: NCT00518245 Terminated - Unstable Angina Clinical Trials

Ischemia Driven Enoxaparin Therapy in ACS Presenting as Low Risk (IDEAL)

IDEAL
Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether enoxaparin (an anticoagulant) is effective in the treatment of patients presenting to the emergency room with chest pain and no electrocardiogram or bloodwork evidence of a heart attack, but with other high risk clinical features

NCT ID: NCT00484406 Completed - Unstable Angina Clinical Trials

MMP Polymorphisms and Acute Coronary Syndromes

Start date: February 2005
Phase: N/A
Study type: Observational

Some Matrix Metalloproteases, proteases degrading the extracellular matrix, play a relevant role in structure and stability of atherosclerotic plaques. Atherosclerotic plaques triggering acute coronary syndromes show increased expression of MMP-1, MMP-3 and MMP-9. Regulation of these MMPs is plaid by genetic polymorphisms, G+/G- at –1563 for MMP-1, 4A/5A- at –1612 for MMP-3, and a microsatellite (13-27 CA repeats around –90) for MMP-9. It is conceivable that these polymorphisms correlate with the clinical outcome of acute coronary syndromes, particularly with those without ST segment Elevation (NSTEACS).

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: NCT00449826 Completed - Clinical trials for Acute Coronary Syndrome

Risk Stratification of Non ST Elevation ACS With Computed Tomographic Angiography (REACT)

Start date: September 2006
Phase: N/A
Study type: Interventional

The purpose of this project is to examine the effectiveness of computed tomographic angiography (CTA) in patients with non-ST elevation acute coronary syndrome (NSTE-ACS). People who are hospitalized with this situation often require an angiogram to assess the heart and its arteries. Recent advancements in technology have enabled CTA to clearly define coronary artery anatomy with great accuracy and to guide treatment strategies in select patient populations. We are investigating that CTA may be used, as an alternative to conventional angiograms, for the risk stratification of patients with high risk NSTE-ACS. Patients eligible for the study will be high risk NSTE-ACS and awaiting an angiogram. Enrolled patients will undergo CTA prior to the angiogram. With each CTA the patient will be injected with a small dose of an X-ray dye and will be asked to lie still on the "scanning bed" for a period of 5-10 minutes.

NCT ID: NCT00372671 Completed - Clinical trials for Myocardial Infarction

Evaluation of an Introductory Videotape Intervention to Improve Cardiac Rehabilitation Participation

Start date: June 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether a pre-discharge videotape introducing the concept and benefit of a Cardiac Rehabiliation & Secondary Prevention (CRSP) program will increase intent to participate in a CRSP program in post myocardial infarction, unstable angina, coronary artery bypass surgery, or coronary angioplasty patients.

NCT ID: NCT00355992 Terminated - Clinical trials for Ischemic Heart Disease

The Ischemia Modified Albumin In Diagnosing Ischemic New Events

IMAgine
Start date: September 2006
Phase: N/A
Study type: Observational

The purpose of the study is to evaluate the utility of Ischemia Modified Albumin (IMA) for risk stratification in patients presenting with chest discomfort and possible ischemic heart disease, and to evaluate the diagnostic and prognostic implication for IMA for major adverse cardiac events.