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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT02498470 Recruiting - Clinical trials for Coronary Artery Disease

Prospective Registry to Assess the Cath Lab Percutaneous Coronary Intervention Long-term Outcomes: a Single Center

PCI-registry
Start date: January 2008
Phase: N/A
Study type: Observational [Patient Registry]

The registry study is to obtain the state of the percutaneous coronary intervention state treatment for coronary heart disease in the center of the first hospital of sun yat-sen unversity in a real world.

NCT ID: NCT02498431 Completed - Clinical trials for Coronary Artery Disease

Serum Irisin in Myocardial Infraction and Following Percutaneous Coronary Intevention

IRICARDIO
Start date: June 2015
Phase: N/A
Study type: Interventional

The investigators aim to evaluate circulating irisin levels alterations in patients with acute myocardial infraction and in patients with coronary artery disease subjected to percutaneous coronary intervention.

NCT ID: NCT02497014 Recruiting - Clinical trials for Coronary Artery Disease

The European Bifurcation Club Left Main Study

EBC MAIN
Start date: February 2016
Phase: N/A
Study type: Interventional

The objective of the study is to investigate clinical outcomes following single versus dual stenting strategies for the treatment of true bifurcation distal left main coronary artery lesions.

NCT ID: NCT02496858 Recruiting - Clinical trials for Coronary Artery Disease

Clinical and Genetic Characteristics of Coronary Artery Disease in Chinese Young Adults

GRAND
Start date: May 12, 2017
Phase:
Study type: Observational

The aim of this study is to identify genetic loci,or gene variations contributing to the development of coronary artery disease (CAD) in Chinese young adults. Investigators will compare coronary angiogram results to genetic findings within young CAD patients.

NCT ID: NCT02496234 Completed - Clinical trials for Coronary Artery Disease

The Use of Aging Biomarkers to Predict Adverse Outcomes After Cardiac Surgery

Start date: July 2015
Phase: N/A
Study type: Observational

Cardiac surgery associated acute kidney injury (CSA-AKI) has been recognized as the second most common cause of hospital acquired AKI. The development of CSA-AKI is independently associated with an increased risk of in-hospital death. There are currently no biomarkers that could identify patients at higher risk for AKI and current risk predictor scores that are based on clinical and demographic information are inadequate. Therefore, a diagnostic test for predicting AKI risk in this clinical context would assist clinicians to optimize surgical strategy and postoperative care to prevent CSA-AKI occurrence and improve patient outcomes. The primary purpose of this study is to measure the association between baseline expression of senescence markers in blood using SenesceTest and the occurrence of CSA-AKI post surgery.

NCT ID: NCT02496169 Not yet recruiting - Clinical trials for Coronary Artery Disease

Prospective multicEntric NonranDomized Registry

ExPEND
Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of the eucaLimus Sirolimus Eluting stent system in patients with de novo coronary lesions.

NCT ID: NCT02494557 Completed - Clinical trials for Coronary Arteriosclerosis

Risk Stratification for Coronary Artery Disease With Type 2 Diabetic Patients

CAD-risk
Start date: September 2014
Phase: N/A
Study type: Observational

Diabetic type 2 patients (DB2) has a higher prevalence of coronary artery disease (CAD) than non-diabetic persons. Presence of CAD results in murmurs arising from the filling of the arteries and can be detected by the CADScor System and can together with biological patient profile indicate the risk of presence of CAD in the patient. In the pilot study 100 asymptomatic DB2-patients examined with CADScor System and biomarkers will be compared with computed tomography (CT) cardiography and single-photon emission computed tomography (SPECT) for assessing if combination of patient profile (gender, age etc) combined with above measures may give rise to new improved risk scoring method for he DB2-patient.

NCT ID: NCT02494284 Terminated - Clinical trials for Coronary Artery Disease

Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Eluting Stent Implantation

STAMP-DES
Start date: December 22, 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare short-term (6-month Dual Anti Platelet Therapy(DAPT) followed by clopidogrel monotherapy) vs. standard long-term dual antiplatelet strategies (24-month DAPT followed by aspirin monotherapy) on clinically relevant bleeding complications (Bleeding Academic Research Consortium(BARC) type 2, 3, or 5)31 in patients after zotarolimus-eluting stent implantation.

NCT ID: NCT02493413 Completed - Obesity Clinical Trials

The Stress-release Effects of Exercise in Obese Are Determined by DS14 Score and T-cell Activation Status

Start date: January 2012
Phase: N/A
Study type: Observational

The purpose of the study was to analyze negative affectivity (NA) and social inhibition (SI) inquired by DS14 score in type D personality (distressed personality) to the relation of autonomic regulation of heart function (HRV) and immune response (T lymphocyte) among obese patients within coronary heart disease group (CHD). As stress is the key psychological activator of the hypothalamic-pituitary-adrenal axis (HPA axis) and therefore an important risk factor for diminished immune competency and prevalence of chronic conditions such as obesity, investigators chose exercise as the stress release intervention, especially as chronic stress may have a role in obesity, related to initiation or exacerbation of the condition. Abnormal regulation of the hypothalamic-pituitary-adrenal axis is additionally associated with chronic inflammatory conditions. Proinflammatory T-lymphocytes are present in visceral adipose tissue and may contribute to local inflammatory cell activation before the appearance of macrophages, suggesting that these cells could play an important role in the initiation and perpetuation of adipose tissue inflammation.

NCT ID: NCT02491931 Completed - Clinical trials for Ischemic Heart Disease

Oral Glutamine in Cardiopulmonary Bypass

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

Introduction: Glutamine (GLN) is the most abundant free amino acid in the body. It modulates immune cell function and is an important energy substrate for most cells (especially for enterocytes and lymphocytes) in critical patients. GLN levels significantly decreased during sepsis/critical illness leading to an increase in infectious complications, organ failure and mortality. Moreover, in cases of ischemia/reperfusion injury in the myocardium, GLN increases the levels of Adenosine triphosphate (ATP)/Adenosine diphosphate (ADP) ratio and prevents intracellular lactate accumulation. Recently, the perioperative effect of intravenous and oral GLN treatment been associated in lowering levels of cardiac injury markers such as Troponin-I (TROP-I) and the number of postoperative complications in patients who underwent Cardiopulmonary Bypass (CPB). The aim of the study was to analyze the oral dose of preoperative oral GLN treatment in patients who underwent CPB with extracorporeal circulation in Mexican patients.