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Acute Myocardial Infarction clinical trials

View clinical trials related to Acute Myocardial Infarction.

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NCT ID: NCT02524964 Recruiting - Clinical trials for Acute Myocardial Infarction

Sodium Tanshinone IIA Sulfonate in Left Ventricular Remodeling Secondary to Acute Myocardial Infarction

Start date: December 2015
Phase: Phase 4
Study type: Interventional

Approximately 60 patients with ST-segment elevation myocardial infarction successfully treated with primary percutaneous coronary intervention will be enrolled and randomized to receive the sodium tanshinone IIA sulfonate in addition to standard therapy or the same volume/day of normal saline. The primary endpoint is the variation in LV end-diastolic volume index (LVEDVi) assessed with cardiac magnetic resonance imaging (MRI) at baseline and 6 months.

NCT ID: NCT02518282 Recruiting - Clinical trials for Myocardial Infarction

High-sensitivity Troponin T in Acute Myocardial Infarction After Cardiac Valvular Surgery

Start date: January 2014
Phase: N/A
Study type: Observational

A measurable degree of heart muscle tissue injury is expected in patients undergoing heart valvular surgery. The level of this injury can be measured by cardiac biomarkers in blood samples. Those biomarkers are used to diagnose an acute myocardial infarction. Postoperative myocardial infarction (MI) is a frequent and important complication after cardiac surgery with high morbidity and mortality. Therefore it is very important to recognize any cardiac event in patients who undergo cardiac surgery. Different diagnostic tools can be used to the diagnosis of acute myocardial infarction; however few is known about the value of high-sensitivity cardiac troponin T (hs-cTn) to diagnose a MI after heart valvular surgery. The aim of this study is to determine the upper reference limit of high-sensitivity troponin T concentration to consider the diagnosis of acute myocardial infarction in patients undergoing heart valvular surgery.

NCT ID: NCT02483494 Recruiting - Clinical trials for Acute Coronary Syndrome

Effectiveness of Advanced Practice Nurse-Led Telehealth on Readmissions

ALTRA
Start date: July 8, 2015
Phase: N/A
Study type: Interventional

Aim. To develop and examine the effectiveness of an APN-led telehealth rehabilitative programme as a transitional nursing therapeutic on readmission rates and health related outcomes amongst patients with Acute Myocardial Infarction (AMI) post discharge. Design. Randomized controlled trial with repeated measures. Methodology. A consecutive sampling of 172 patients with AMI will be recruited from a tertiary hospital in Singapore. Participants will be randomised into two groups. The experimental group (ALTRA) will receive APN-led telehealth rehabilitative programme upon discharge in addition to standard care. The control group will receive only standard follow-up care.

NCT ID: NCT02281305 Recruiting - Clinical trials for Acute Myocardial Infarction

Post-MI PET Scan Imaging of Inflammation

Start date: October 2014
Phase: Phase 4
Study type: Interventional

Restoring the patency of the coronary vessels and providing the ischemic myocardium with reperfused blood can cause additional tissue damage. A key element of ischemia and reperfusion (I/R) injury and major determinant of the evolution of damage in the affected myocardium is the inflammatory response. The main objective of the study is to evaluate the efficacy of colchicine in reducing I/R injury by effectively modulating the inflammatory response in the reperfused myocardium.

NCT ID: NCT02071342 Recruiting - Clinical trials for Acute Myocardial Infarction

Study of ABSORB Stent in Acute Myocardial Infarction

ABSORB-ACS
Start date: September 2013
Phase: N/A
Study type: Observational

The aim of our study is to evaluate the clinical outcomes at 30 days and 1 year (cardiac death, myocardial infarction, target lesion revascularization (TLR), target vessel revascularization (TVR), thrombosis of the device in patients who are undergoing angioplasty in myocardial infarction and in which bioabsorbable stent was implanted (BVS). Additionally, we will evaluate the acute recoil after implantation of bioabsorbable stents. A 24 months follow-up , by means of coronary angiography accompanied by QCA and assessment with intracoronary ultrasound (IVUS) and VH (virtual histology) is scheduled.

NCT ID: NCT02001363 Recruiting - Clinical trials for Acute Myocardial Infarction

Efficacy Study of Glucagonlike Peptide-1 to Treat Reperfusion Injury

Start date: November 2013
Phase: N/A
Study type: Interventional

The investigators planned to research the cardioprotective effects of intravenous liraglutide on reperfusion injury.

NCT ID: NCT01971619 Recruiting - Clinical trials for Acute Myocardial Infarction

Association of Vitamin D, Parathyroid Hormone and Fibroblast Growth Factor-23 With Infarction-related Arrhythmia in Patients With Acute Myocardial Infarction

Start date: August 2013
Phase: N/A
Study type: Observational

To investigate the effect of vitamin D deficiency on the development of arrhythmia in patients with acute myocardial infarction.

NCT ID: NCT01936285 Recruiting - Clinical trials for Acute Myocardial Infarction

Colchicine in ST-elevation Myocardial Infarction

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

- There is evidence that inflammatory processes may play detrimental role during the acute phase of myocardial infarction - The hypothesis of this study is that colchicine, by its anti-inflammatory action, may lead to reduction in infarct size, when administered during the acute phase of myocardial infarction

NCT ID: NCT01924507 Recruiting - Clinical trials for Acute Myocardial Infarction

Bedside Sleep Medicine

Start date: August 2013
Phase: N/A
Study type: Interventional

The investigators aimed to evaluated the role of bedside sleep medicine in an cardiology intensive care unit. The patients will be submitted to a overnight polysomnography. Those individuals with sleep apnea will be treated with CPAP during the ICU admission. Also, the investigators will identify the factors that compromise the sleep and will act to minimize them to improve the sleep quality. After the interventions, the investigators will evaluate if there are reduced days of hospital admission, major cardiovascular events (infarction, reinfarction, heart failure and stroke) and overall mortality.

NCT ID: NCT01914055 Recruiting - Clinical trials for Acute Myocardial Infarction

Dissecting the Role of Distal Embolization of Athero-thrombotic Material in Primary PCI: the ThrombOticBurden and mIcrovAscularobStruction (TOBIAS) Study.

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

demonstrate that FD-OCT guidance is feasible and possibly results in reduction of frequency-domain Optical Coherence Tomography-defined residual thrombus burden after thrombus-aspiration.