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Acute Myocardial Infarction clinical trials

View clinical trials related to Acute Myocardial Infarction.

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NCT ID: NCT00212056 Completed - Clinical trials for Acute Myocardial Infarction

Japan-Working Groups of Acute Myocardial Infarction for the Reduction of Necrotic Damage by ANP

Start date: October 2001
Phase: N/A
Study type: Interventional

To evaluate whether ANP as an adjunctive therapy for AMI reduces myocardial infarct size and improves regional wall motion.

NCT ID: NCT00212030 Completed - Clinical trials for Acute Myocardial Infarction

Japan-Working Groups of Acute Myocardial Infarction for the Reduction of Necrotic Damage by a K-ATP

Start date: October 2001
Phase: N/A
Study type: Interventional

To evaluate whether nicorandil as an adjunctive therapy for AMI reduces myocardial infarct size and improves regional wall motion

NCT ID: NCT00209144 Completed - Clinical trials for Acute Myocardial Infarction

Phase 1 Study of Potential Anti-Inflammatory Effects of Glucose Control During Acute Myocardial Infarction.

Start date: October 2004
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if intense control of high glucose levels in patients treated with angioplasty for heart attack has anti-inflammatory and anti-thrombotic effects.

NCT ID: NCT00206830 Completed - Heart Failure Clinical Trials

SHORTness of Breath In the Emergency Department (SHORTIE)

Start date: April 2005
Phase: Phase 2/Phase 3
Study type: Interventional

SHORTIE is a two-phase study to determine the impact of the Triage Profiler S.O.B. (Shortness Of Breath) Panel on patient management, outcome, and cost.

NCT ID: NCT00191282 Completed - Clinical trials for Diabetes Mellitus, Type 2

Hyperglycemia and Cardiovascular Outcomes With Type 2 Diabetes

IONM
Start date: October 2002
Phase: Phase 4
Study type: Interventional

The primary objective was to demonstrate a difference between two insulin strategies, one targeting postprandial (PP) hyperglycemia and the other targeting fasting and interprandial hyperglycemia, on time until the first combined adjudicated cardiovascular (CV) event (primary outcome defined as CV death, nonfatal myocardial infarction [MI], nonfatal stroke, coronary revascularization, or hospitalized acute coronary syndrome).

NCT ID: NCT00187460 Completed - Clinical trials for Acute Myocardial Infarction

Study of the Effectiveness of Report Cards on the Quality of Care for Heart Attack and Heart Failure Patients

EFFECT
Start date: November 2001
Phase: N/A
Study type: Interventional

Randomized cluster trial of cardiac report cards for AMI and CHF. 103 acute care Ontario hospitals/85 hospital corporations participating, randomized to two groups: Group A Early Feedback and Group B Delayed Feedback. Two phases of retrospective chart review of AMI and CHF separations to assess the impact of the public release of hospital specific performance on a set of Canadian quality indicators.

NCT ID: NCT00178620 Completed - Clinical trials for Myocardial Infarction

Pre-hospital Administration of Thrombolytic Therapy With Urgent Culprit Artery Revascularization

PATCAR
Start date: September 2003
Phase: Phase 4
Study type: Interventional

The PATCAR study has been designed to test the hypothesis that the strategy of pre-hospital use of a "clot busting" (thrombolytic) drug followed with emergent heart catheterization including stenting of the problematic coronary artery, will result in a lower mortality and reduced repeat heart attack rates. Early identifying and treating heart attacks patients prior to the arriving at the hospital, in those patients who qualify for the "clot busting" drugs will lower the size of the heart attack damage. This smaller heart attack will lead to fewer problems with less repeat heart attacks and death in the future.

NCT ID: NCT00175942 Recruiting - Clinical trials for Acute Myocardial Infarction

Risk Indicators in Patients With Ventricular Fibrillation During Acute Myocardial Infarction

Start date: February 2003
Phase: N/A
Study type: Observational

Sudden cardiac death is in most cases triggered by ischemia-related ventricular tachyarrhythmias and accounts for 50% of deaths from cardiovascular disease in developed countries. Chronic elevation of indicators of coagulation activation has been found in patients with coronary heart disease , but a role of coagulation activation and proinflammatory state as a potential risk factor for ventricular fibrillation (VF) during acute myocardial infarction has not been investigated.

NCT ID: NCT00161005 Unknown status - Clinical trials for Acute Myocardial Infarction

Norwegian Study on District Treatment of ST-Elevation Myocardial Infarction

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

In the district areas of Norway patients with acute myocardial infarction with ST-elevation, are treated with thrombolysis. An increasing part of them receives thrombolysis before arrival to the local hospital.Usually these patients have been sent to an invasive center if thrombolysis fails or the patient gets ischemic symptoms during the stay. This study will compare this strategy against immediate transportation to an invasive center after the patient has received thrombolysis.

NCT ID: NCT00157768 Completed - Clinical trials for Acute Myocardial Infarction

IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute Myocardial Infarction

Start date: June 9, 1999
Phase: Phase 4
Study type: Interventional

Of the patients who survive hospitalization after an acute myocardial infarction, ca. 10% die of sudden cardiac death in the following 2 years. The prognosis appears not improved by medication with antiarrhythmics (class I/III). A positive effect of beta-blockers (Metoprolol CR/Zok) on total mortality after myocardial infarction in patients with heart failure is well established. On the other hand, an implantable defibrillator (ICD) proved to be superior to medication when used for secondary prevention in patients after cardiac arrest. The question arises whether ICD therapy is also effective in primary prevention in high risk patients after acute myocardial infarction. This study determines if patients, who were defined as high risk patients in the early post infarction phase by means of noninvasive methods, benefit from primary prevention by means of an ICD. Special emphasis is put on an individual optimization of the infarction therapy, including beta-blockers.