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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT02089867 Completed - Clinical trials for Coronary Artery Disease

Plant Sterols Effect on Previous Statin Therapy

Start date: October 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the effect of plant sterols associated with ezetimibe in LDL-cholesterol levels in coronary patients previously on statin therapy

NCT ID: NCT02086617 Completed - Clinical trials for Abdominal Aortic Aneurysm

Screening of Abdominal Aortic Aneurysms Among Men With Coronary Artery Disease

Start date: March 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate prevalence of abdominal aortic aneurysms (AAA) among male patients with coronary artery disease (CAD). Secondary purpose is to document cost-effectiveness of ultrasound screening of AAA in selected population. Ethiology of AAA is known to be common with atherosclerotic arterial diseases, and on the basis of our previous studies (ClinicalTrials.gov ID CAD-AAA-02) the prevalence of AAA seems to be higher in CAD population than unselected male population. This leads to hypothesis that selective screening of these patients (for AAA) could be cost-efficient and life saving option for detecting AAAs before rupture. Study will be carried out as a single-center prospective screening study. Patients will be selected for this study on basis of their ICD 10 diagnose codes in North Carelian patient information system. Inclusion criteria will be any kind of atherosclerotic heart disease (ICD10 codes I20-I25). Criteria for exclusion are malignant disease, already diagnosed or treated AAA and failure to give informed consent. 800 patient records that meet the inclusion criteria will be reviewed for eligibility. Invitations for screening will be sent for 600 patients with intention to have at least 400 patients screened. Screening will be done by verified sonographers in designated screening appointments.

NCT ID: NCT02086045 Completed - Clinical trials for Coronary Artery Disease

Elixir Medical Clinical Evaluation of the DESolve® Novolimus Eluting Bioresorbable Coronary Scaffold System - The DESolve Nx Trial

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

To evaluate the safety, performance and efficacy of the Elixir DESolve® Novolimus Eluting Bioresorbable Coronary Scaffold System (BCSS) in patients with a single de novo native coronary artery lesion designated the target lesion and up to one non-target lesion located in a separate epicardial vessel.

NCT ID: NCT02086006 Completed - Clinical trials for Coronary Artery Disease

Elixir Medical Clinical Evaluation of the DESolve Myolimus Eluting Bioresorbable Coronary Stent System - DESolve I Trial

Start date: February 2011
Phase: N/A
Study type: Interventional

This prospective, consecutive enrolment, single-arm study will enroll up to 15 patients with single de novo, Type A lesions < 10 mm in length and located in a native coronary artery with a reference vessel diameter of 2.75 mm - 3.0 mm as measured by both offline QCA and IVUS. All patients will receive a 3.0 x 14mm DESolve Stent loaded with approximately 40 mcg of Myolimus. - Angiographic and intravascular ultrasound (IVUS) will be completed for all patients at baseline and at 6 months. - Optical Coherence Tomography (OCT) will will be completed for all patients at baseline and at 6 months. - Multi-slice computed tomography (MSCT) will be conducted on all patients enrolled at 12 and 24 months.

NCT ID: NCT02084888 Completed - Clinical trials for Coronary Artery Disease

Prognostic Impact of Chronic Total Occlusions

Start date: January 2005
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to determine the prognostic impact of the presence of chronic total occlusions (CTO) of the coronary arteries in patients undergoing coronary angiography and PCI.

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: NCT02082483 Completed - Clinical trials for Coronary Artery Disease

Coronary Artery Disease Screening in Kidney Transplant Candidates

CADScreening
Start date: November 2014
Phase: N/A
Study type: Interventional

Kidney transplant candidates are at very high risk for coronary artery disease (CAD). The optimal strategy to monitor and maintain the cardiac fitness of patients awaiting kidney transplantation is unknown. Currently patients undergo annual testing; however, screening for CAD may increase morbidity and mortality by: 1. exposing patients to the risk of angiography and revascularization procedures 2. delaying or excluding patients from life saving transplantation. Before proceeding with a definitive study to determine whether screening is necessary, feasibility will be determined in this pilot study.

NCT ID: NCT02081443 Completed - Clinical trials for Coronary Artery Disease

In Vitro Pharmacodynamic Effects of Cangrelor in Ticagrelor Treated Patients

Start date: April 2014
Phase: N/A
Study type: Interventional

Cangrelor is a potent intravenous P2Y12 receptor inhibitor with rapid onset and offset of action associated with a greater reduction in ischemic events, including stent thrombosis, in patients undergoing stent procedures who have not been pretreated with clopidogrel. In vitro investigations have shown cangrelor to be associated with more rapid, potent, and consistent platelet inhibition in patients on maintenance prasugrel therapy exposed to a re-loading dose of prasugrel. However, if cangrelor exerts similar effects in ticagrelor treated patients remain unknown. The aim of the present study is to evaluate the effects on platelet function achieved after in vitro incubation with cangrelor in patients on ticagrelor maintenance dose who receive a loading dose of ticagrelor.

NCT ID: NCT02079194 Active, not recruiting - Clinical trials for Coronary Artery Disease

Comparison Between P2Y12 Antagonist Monotherapy and Dual Antiplatelet Therapy After DES

SMART-CHOICE
Start date: March 18, 2014
Phase: N/A
Study type: Interventional

To compare the efficacy and safety of clopidogrel monotherapy versus aspirin plus P2Y12 antagonist following 3-month of DAPT in patients undergoing PCI with DES.

NCT ID: NCT02077218 Completed - Hypertension Clinical Trials

Computed Tomography and Biomarker Analysis in Diagnosing Coronary Artery Disease in Asymptomatic Patients Who Have Undergone Stem Cell Transplant

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

This pilot clinical trial studies computed tomography (CT) scans and biomarker analysis in diagnosing coronary artery disease (CAD) in patients who have undergone a stem cell transplant but have no symptoms of CAD. CAD is a disease in which there is a narrowing or blockage of the coronary arteries (blood vessels that carry blood and oxygen to the heart) and patients who have undergone a stem cell transplant are at an especially high risk for CAD. A CT scan involves a series of detailed pictures of areas inside the body taken from different angles. The pictures are created by a computer linked to an x-ray machine. Studying samples of blood from patients who have undergone a stem cell transplant in the laboratory may help doctors identify and learn more about biomarkers related to CAD. Using a CT scan in combination with biomarker analysis may be a better and less-invasive way to diagnose CAD.