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Active clinical trials for "Coronary Artery Disease"

Results 801-810 of 4926

Clinical Outcomes of Patients Undergoing CABG Surgery With VEST Supported Venous Grafts

Coronary Artery Disease

This is a prospective, investigator-initiated, multi-center, open label and post-market registry, enrolling patients with atherosclerotic coronary artery disease, scheduled for CABG with at least one SVG bypass. The registry is designed to evaluate the clinical outcome of CABG surgery with an external support device (VEST) for SVG bypasses. In each patient, use of the VEST will be according to its approved indications for use and attempt will be made (based on clinical judgement) to support each non-sequential SVG bypass graft with a VEST device. Subjects will be followed for 5 years, with interim follow ups at 12 and 24 months. MACCE and EQ5D3L will be documented at every follow up visit.

Recruiting6 enrollment criteria

Perioperative Troponin I and NT Pro-BNP in Lung Resection

Cardiac IschemiaThoracic Cancer1 more

After lung resection, troponin elevation may be regulated by mechanisms other than myocardial ischemia. Perioperative natriuretic peptides measurement may help identify changes in ventricular function during thoracic surgery. Integrating both cardiac biomarkers may improve the predictive value for cardiovascular complications after lung resection.

Recruiting4 enrollment criteria

Essen Coronary Artery Disease Registry

Coronary Artery Disease

The ECAD registry is a registry of patients undergoing coronary angiography at the West German Heart and Vascular Center. The registry anticipates to determine predictors of patient outcome after coronary angiography.

Recruiting2 enrollment criteria

Residual Inflammation and Plaque Progression Long-term Evaluation

AtherosclerosisMyocardial Infarction2 more

Inflammation drives atherosclerotic plaque rupture triggering most acute coronary syndromes. Despite advances in diagnosis and management of atherosclerosis, patients with myocardial infarction (MI) remain at increased risk of recurrent events. The RIPPLE study aims to examine the relationship between residual coronary inflammation detected by 68Ga-DOTATATE PET in patients treated for MI to long-term plaque progression measured by CT coronary angiography (CTCA). The association between infarct-related myocardial 68Ga-DOTATATE PET and myocardial function and viability will also be assessed.

Recruiting15 enrollment criteria

Screen of DM by OGTT in Subjects Receiving CAG or MDCT for CAD

Diabetes MellitusCoronary Artery Disease

To determine the glucose regulation status of patients who were suspected to have CAD in central Taiwan.

Recruiting5 enrollment criteria

Comparison of Troponin Assay With New POCT Method in the Decision-making Pathway of Patient With...

Chest PainMyocardial Ischemia

This is a prospective observational study aiming to evaluate the diagnostic accuracy of the high-sensitivity Troponin assay performed with the Atellica VTLi POCT system (by comparison with the results obtained with the Atellica diagnostic system currently in use) and to evaluate the impact of the POCT system on the reduction of decision-making time (particularly of "rule-out"), by evaluating the number of cases in which the conclusion of the decision pathway at 3 h (algorithm currently in use) could have been concluded at 1 h.

Recruiting5 enrollment criteria

A Registry Study of Biomarkers in Ischemic Heart Disease ( BIOMS-IHD )

Cardiovascular Diseases

The registry study aims to discover biomarkers for accurate classification and risk assessment of ischemic heart disease.

Recruiting6 enrollment criteria

iFR Guided Coronary Artery Bypass Grafting Surgery

Ischaemic Heart DiseaseCoronary Artery Disease1 more

The expected outcome of better and improved patency of bypass grafts and its direct relation to pre-operative iFR measurements of stenosis as compared to direct visual physiology of stenosis in the coronary angiogram. To establish the correlation between the use of intracoronary physiology and improved graft patency at 12 months for patients undergoing CABG surgery. It is a minimum of 28 and a maximum of 100 patients single-centre proof or concept/ observational study/ pilot study.

Recruiting7 enrollment criteria

Leg Ischaemia Management Collaboration

Peripheral Arterial DiseaseCritical Limb Ischemia3 more

Single-centre prospective cohort study of patients presenting with severe limb ischaemia (SLI). The primary outcome measure will be 12 month major amputation rate. A historical cohort of patients identified retrospectively will be the comparitor group used to assess the impact of a newly-established rapid-access limb salvage clinic. Primary aim: - Determine the proportion of patients with SLI undergoing major lower limb amputation within 12 months of presentation. Secondary aims: Assess clinically important short-, medium- and long-term outcomes in those undergoing and not undergoing amputation Prevalence and degree of frailty and cognitive impairment Pevalence and degree of cardiac disease (detected by stress MRI) Establish a biobank for future biomarker analysis Investigate the role of frailty and cognitive assessments, cardiac MRI and biomarkers in risk-stratification of patients with SLI

Recruiting19 enrollment criteria

Myocardial Perfusion Imaging by 15O-H2O PET/CT

Ischemic Heart Disease

The trial will include 2500 patients with evident or suspected ischemic heart disease refered to Department of Nuclear Medicine & PET Centre, Aarhus University Hospital, for perfusion imaging by 15O-H2O PET/CT scan of the heart during rest and stress. The patients will undergo the clinical scan as normal. Data from the scans will be used to determine reference values of the examination. Follow up will be done for up to 10 years in regards to major cardiovascular events in order to determine the prognostic value of the scan.

Recruiting2 enrollment criteria
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