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Myocardial Ischemia clinical trials

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NCT ID: NCT02060357 Completed - Clinical trials for Coronary Artery Disease

Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes (OCT-DES)

OCT-DES
Start date: November 2011
Phase: N/A
Study type: Interventional

The aim of this study is a comparative evaluation of re-endothelailisation of the Integrity Resolute zotarolimus eluting stent (Medtronic) and of the Promus Element erolimus eluting stent (Boston Scientific), in patients with diabetes. We plan to compare endothelial coverage and neointimal proliferation using OCT and compare this data to published results from conventional stents.

NCT ID: NCT02059993 Completed - Hypertension Clinical Trials

The Effects of Obstructive Sleep Apnea and Its Intervention on Coronary Heart Disease

Start date: January 2009
Phase: N/A
Study type: Interventional

Obstructive sleep apnea(OSA) is an important identifiable cause of hypertension. Previous study has suggested that OSA significantly increases cardiovascular morbidity and mortality, especially in patients with pre-existing cardiovascular disease.The standardized treatment of moderate/severe OSA is continuous positive airway pressure (CPAP). Most of short-term trials indicated that CPAP treatment reduced BP in patients with OSA. But relevant studies have a relative short duration with only but few more than one year. In our opinion, they are not sufficient to detect the real effect of CPAP on reduction in BP. Besides, the impact of OSA on metabolic disorder is still unclear.We hypothesized that long-term CPAP treatment could reduce blood pressure and improve metabolic disorder in patients with coronary heart disease (CHD)and OSA.

NCT ID: NCT02059681 Completed - Clinical trials for Chronic Myocardial Ischemia

Phase I Trial of Endocavitary Injection of Bone Marrow Derived CD133+ Cells in Ischemic Refractory Cardiomyopathy (RECARDIO Trial)

RECARDIO
Start date: December 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate whether endocavitary intramyocardial injection of autologous bone-marrow-derived CD133+ cells is safe on the basis of number of adverse events, with follow-up assessments extending up to 1 year after enrolment.

NCT ID: NCT02059512 Completed - Clinical trials for Ischemic Heart Disease

Autologous Bone Marrow Mononuclear Cells in the Combined Treatment of Coronary Heart Disease

TAMIS
Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this study evaluate the effect of the method of administration of autologous bone marrow mononuclear cells for the duration of of functioning aorto-coronary bypass grafts in the surgical treatment of coronary heart disease, to assess the degree of effectiveness depending on the method of transplantation (intramyocardial, intracoronary, combined).

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: NCT02057978 Completed - Clinical trials for Coronary Artery Disease

EXCEL-II Stent Vesus EXCEL Stent to Treat the Patients With de Novo Coronary Artery Lesions.

CREDIT-II
Start date: December 8, 2013
Phase:
Study type: Observational [Patient Registry]

The purpose of this Randomized Study to evaluate the safety and efficacy of the Excel-II DES compared to the EXCEL DES in the treatment of patients with de novo coronary artery lesions.

NCT ID: NCT02057900 Completed - Clinical trials for Ischemic Heart Disease

Transplantation of Human Embryonic Stem Cell-derived Progenitors in Severe Heart Failure

ESCORT
Start date: May 27, 2013
Phase: Phase 1
Study type: Interventional

The purpose of the study is to assess the feasibility and safety of a transplantation of cardiac-committed progenitor cells derived from human embryonic stem cells in patients with severe heart failure.

NCT ID: NCT02055443 Completed - Chest Pain Clinical Trials

Myocardial Ischemia Detection for Early Identification of Patients With Ischemic Chest Pain

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

The purpose of this study is to evaluate whether new novel markers from the clinical electrocardiogram (EKG), which have been used as non-invasive measures of heart disease, can detect coronary artery disease in patients with chest pain. The researchers are especially interested in studying how changes in these unique waves evolve over time with rest and activity. It is hoped that the findings will be helpful in differentiating patients with cardiac chest pain at emergency departments from those with non-cardiac chest pain, as early identification can accelerate treatment and save lives. Eligible participants are those age 18 and older who have been referred for a nuclear stress test at University of Pittsburgh Medical Center Presbyterian Hospital to rule out coronary artery disease as part of their clinical care.

NCT ID: NCT02054988 Recruiting - Clinical trials for CORONARY ARTERY DISEASE

"Potential Effect of Acute and Chronic Caffeine Administration on Platelet Reactivity in Patient With Coronary Artery Disease on Dual Antiplatelet Therapy"

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

Prasugrel is a potent thienopyridine antiplatelet agent that selectively and irreversibly inhibits ADP-induced platelet aggregation mediated by the P2Y12 receptor. Prasugrel is a prodrug that must first undergo biotransformation to its active metabolite via cytochrome P450-mediated hepatic metabolism (CYP1A2). Clopidogrel is currently administered to several million patients especially after coronary stenting. Clopidogrel has been shown to reduce cardiovascular complications in patients with acute coronary syndromes and patients who have undergone coronary stenting. The mechanism of action of clopidogrel's active metabolite involves inhibition of the purinergic adenosine diphosphate (ADP) receptor P2Y12 on the platelet membrane. Blockade of this receptor prevents uncoupling of the associated Gi2 protein which ultimately leads to increased platelet cyclic AMP (cAMP) formation.3 Cyclic AMP is a key signaling molecule in inhibiting platelet aggregation, but its intracellular levels are affected by several other commonly used compounds. For instance, methylxanthines, such as caffeine, theophylline, and theobromine (an ingredient of chocolate), all cause elevation of intracellular cAMP levels by inhibiting adenosine receptors (types A1 and A2) on the platelet membrane. The effect of caffeine consumption on platelet reactivity depends on the caffeine dose and duration of administration. Chronic caffeine consumption (≥7 days) appears to be associated with inhibition of platelet aggregation, probably through upregulation of adenosine receptors.The aim of this study was to examine the effect of acute caffeine consumption, at a dose equivalent to commercial coffee drinks, on the antiplatelet effect of clopidogrel and prasugrel, in patients with coronary artery disease (CAD). Platelet function will be evaluated using a validated method: the VerifyNow System (Accumetrics Inc., San Diego, CA), which is a point-of-care turbidimetry-based optical detection system that measures platelet-induced aggregation.

NCT ID: NCT02054390 Completed - Clinical trials for Coronary Artery Disease

Angiotensin Converting Enzyme Inhibitors and Periprocedural Myocardial Infarction

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

Metabolic syndrome (MS) has been reported as a risk for cardiovascular events. The aim of the present cohort study is to investigate whether ACEi therapy reduces the rate of periprocedural myocardial injury (PPMI) after elective percutaneous coronary intervention (PCI) among patients with metabolic syndrome.