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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT02207270 Terminated - Clinical trials for Coronary Artery Disease

Study Of Costs Realized After Percutaneous Coronary intervenTion Employing Same Day Discharge

SOCRATES
Start date: August 11, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the total costs of care associated with uncomplicated elective or low-risk urgent percutaneous coronary intervention (PCI) through 30-day follow up are lower among patients who are randomly assigned to same day discharge (SDD) or overnight hospital stay (ON).

NCT ID: NCT02205775 Terminated - Clinical trials for Stable Coronary Artery Disease Undergoing PCI

Rosuvastatin for Reduction of Myocardial Damage and Systemic Inflammation During Coronary Angioplasty

REMEDY
Start date: May 2010
Phase: Phase 3
Study type: Interventional

Myocardial necrosis is relatively frequent after percutaneous coronary intervention and is associated with higher mortality during the follow-up. Since anti-inflammatory properties of statins have been demonstrated and the benefit of statins in acute coronary syndromes have been proven, this study aims at testing the hypothesis that the pre-procedural intensive statin treatment reduce the extent of peri-procedural necrosis.

NCT ID: NCT02136758 Terminated - Obesity Clinical Trials

Cardiovascular Risk Clinic

CRC
Start date: April 2009
Phase: N/A
Study type: Interventional

This study was a prospective, randomized trial designed to investigate the efficacy of moderate lifestyle modification for improving the clinical status of patients with coronary artery disease or patients with risk factors that promote coronary artery disease.

NCT ID: NCT02121158 Terminated - Clinical trials for Coronary Artery Disease

Efficacy and Safety of Implantable Cardioverter-Defibrillator (ICD) Implantation in the Elderly

I-70
Start date: August 7, 2015
Phase: N/A
Study type: Interventional

The overall aim of this trial is to study the safety and efficacy of ICD implantation as a primary prevention strategy of sudden cardiac death in patients 70 years and older. This study will assess the many competing factors involved with ICD implantation including 1) the impact on mortality, especially in the context of a declining rate of sudden death with advanced age, 2) the tolerability of the powerful therapeutic action of the device, and 3) the impact on quality of life.

NCT ID: NCT02105623 Terminated - Clinical trials for Coronary Arteriosclerosis

EARly Prevention of aTHeroma Progression

EARTH
Start date: June 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare standard therapy (risk factor control, life style modification) versus standard therapy plus low-dose rosuvastatin therapy (5mg/day) on progression of coronary atherosclerosis in statin naive individuals who have mild CAD (nonobstructive coronary atherosclerotic plaques) and normal LDL (low-density lipoprotein) cholesterol levels(〈130mg/dl).

NCT ID: NCT02102997 Terminated - Clinical trials for Coronary Artery Disease

Deutsches Dual Therapy Stent Register

DTS Register
Start date: July 2013
Phase: N/A
Study type: Observational [Patient Registry]

The DTS.DE registry is an initiative for the collection of high quality process and historical data of implantations with the COMBO Dual Therapy Stent in Germany. DTS.DE was designed as a national, non- randomized, prospective, multicenter registry without a comparison group. The responsible Steering Committee is of the opinion that the Combo stent qualifies for further documentation of treatment results in the form of a German registry, based the CE certification of the COMBO Dual Therapy stent in 2013 and its clinical and scientific investigation in the context of the REMEDEE study program, as well as company independent externally initiated studies with the COMBO Dual Therapy Stent. It is expected that by mid- 2015, at least 1,000 patients will be enrolled and documented in the DTS.DE registry with the COMBO Dual Therapy Stent. A clinical follow-up is performed after 6 weeks and 12 months.

NCT ID: NCT02083146 Terminated - Clinical trials for Coronary Artery Disease (CAD)

C1q/TNF-related Proteins in Coronary Artery Disease

Start date: March 2011
Phase:
Study type: Observational

Now, adipose tissue is established as an active endocrine organ that controls systemic energy homeostasis by secretion of adipokines. Recently, members of the C1q/tumor necrosis factor-related protein (CTRP) family have been reported to share structural homology with adiponectin. To date, 15 CTRP family members have been found that might play major roles in metabolism and inflammation. The investigators tried to clarify the relationship between CTRP family and coronary artery disease (CAD) in Korean men and women.

NCT ID: NCT02061696 Terminated - Clinical trials for Coronary Artery Disease

ARISTOCRAT-A Randomized Controlled Trial Evaluating Closure Following Access With the AXERA (Device Name) 2 Access System

ARISTOCRAT
Start date: January 2014
Phase: N/A
Study type: Interventional

The goal of the research study is to observe the clinical safety, effectiveness and patient satisfaction of the AXERA 2 Access System in subjects undergoing coronary angiographic and possible Percutaneous Coronary Intervention (PCI) through the femoral artery when compared to standard manual compression.

NCT ID: NCT02058134 Terminated - Clinical trials for Coronary Artery Disease

The CardioPAT Project: A Randomized Trial

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

The purpose of this study is to determine whether intra- and postoperative use of the cardioPAT® cell saver decreases the need for allogenic red blood cell transfusion in patients, who undergo open heart surgery (with cardiopulmonary bypass) and preoperatively have an increased risk for bleeding.

NCT ID: NCT02045134 Terminated - Clinical trials for Coronary Heart Disease

Supplementation With Polyphenol-Rich Foods and Atrial Fibrillation After a Cardiac Surgery

Polyphemus
Start date: September 2014
Phase: N/A
Study type: Interventional

Post-operative atrial fibrillation (POAF) is a major cause of morbidity and mortality after a cardiac surgery. Both systemic inflammation and oxidative stress play a role in the initiation of POAF after a cardiac surgery. Epidemiological studies show a significant inverse correlation between cardiovascular risk and consumption of polyphenol-rich foods (PRFs), due to antioxidant, vasorelaxant and antithrombotic properties of their polyphenolic components. The main objective of this study is to evaluate the effect of polyphenol-rich food supplementation on post-operative atrial fibrillation (POAF) in patients undergoing an open heart surgery (mainly coronary artery bypass grafts (CABG) and valve replacement or repaired (VR))