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Coronary Disease clinical trials

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NCT ID: NCT01521468 Completed - Clinical trials for Coronary Artery Disease

Comparison of Cardiac Imaging Techniques for Diagnosing Coronary Artery Disease

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

A large number of cardiac catheterizations are performed each year, primarily to diagnose heart disease. However, a cardiac catheterization is an invasive procedure which is associated with serious complications such as heart infarction, stroke, and death. Therefore, there is a need for non-invasive procedures to diagnose coronary heart disease. The purpose of this study is, therefore, to assess the diagnostic accuracy of non-invasive cardiac imaging modalities for the detection of heart disease in patients presenting for the first time to the cardiologist with chest pain.

NCT ID: NCT01519245 Completed - Clinical trials for Coronary Artery Disease

Topical Application of Tranexamic Acid to Reduce Post-operative Bleeding in Coronary Artery Bypass Surgery

Start date: December 2011
Phase: Phase 3
Study type: Interventional

The goal of this project is to determine whether the use of tranexamic acid, a clot-promoting drug, applied topically over the heart in coronary artery bypass graft surgery (CABG) will reduce post operative blood loss. The investigators' hypothesis is that the use of a tranexamic acid-containing cardiac bath prior to chest closure will result in a statistically significant reduction in blood loss and transfusion requirements in patients who undergo CABG.

NCT ID: NCT01518777 Completed - Clinical trials for Coronary Artery Disease

Reducing Radioisotope Dose: the Half-Dose CZT Study

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

This is a pilot study to see whether cardiac imaging can be performed using half the standard dose of radioisotope.

NCT ID: NCT01516541 Completed - Clinical trials for Cardiovascular Disease, Coronary Heart Disease, Dyslipidemia, Peripheral Arterial Disease (PAD)

A Study of Dalcetrapib in Patients With Stable Coronary Heart Disease, With Coronary Heart Disease Risk Equivalents or at Elevated Risk for Cardiovascular Disease

Start date: January 2012
Phase: Phase 3
Study type: Interventional

This multicenter, randomized, double-blind, placebo-controlled, parallel-group study will evaluate the potential of dalcetrapib to reduce cardiovascular morbidity and mortality in patients with stable coronary heart disease (CHD), with CHD risk equivalents or at elevated risk for cardiovascular disease. Eligible patients will be randomized to receive either dalcetrapib 600 mg orally daily or placebo orally daily, on a background of contemporary, guidelines-based medical care. Anticipated time on study treatment is 4 years.

NCT ID: NCT01515228 Completed - Clinical trials for Coronary Artery Disease

Comparison of Cilotax Stent and Everolimus -Eluting Stent With Diabetes Mellitus (ESSENCE-DM III)

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine the safety and effectiveness of coronary stenting with the Cilotax stent compared to the Xience Prime stent in the treatment of diabetic patients.

NCT ID: NCT01515033 Completed - Clinical trials for Coronary Artery Disease

Aerobic Exercise on PETCO2 Response in Coronary Artery Disease Patients

Start date: September 2010
Phase: Phase 2
Study type: Interventional

The purpose of the present study was to evaluate: 1) the effects of continuous exercise training and interval exercise training on end-tidal carbon dioxide pressure (PETCO2) response during graded exercise test in patients with coronary artery disease; and 2) examine the effects of exercise training modalities on the association among PETCO2 at ventilatory anaerobic threshold (VAT) and indicators of ventilatory efficiency and cardiorespiratory fitness in patients with coronary artery disease.

NCT ID: NCT01514656 Completed - Coronary Disease Clinical Trials

CPR Training: Video Self-Instruction Kit or Video-Only

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

Prompt delivery of cardiopulmonary resuscitation (CPR) is a crucial determinant of survival for many victims of sudden cardiac arrest (SCA), yet bystander CPR is provided in less than one third of witnessed SCA events. A number of barriers to bystander CPR training have been identified including time and cost of the training course. Since the large majority of arrest events occur in the home environment, studies have suggested that providing CPR training to family members of hospitalized cardiac patients may serve as a useful approach to address an environment in which bystander CPR is frequently not provided. Utilizing an existing in-hospital program to train adult family members, the investigators will assess the skills of those who learn CPR through two different education methods (video-only and video self-instruction (VSI) kit).

NCT ID: NCT01514227 Completed - Clinical trials for Coronary Artery Disease

Nobori Dual Antiplatelet Therapy as Appropriate Duration

Start date: December 2011
Phase: Phase 4
Study type: Interventional

NIPPON trial is a prospective, randomized, trial comparing 6 and 18 months Dual Antiplatelet Therapy (DAPT) following Nobori stent deployment.

NCT ID: NCT01513070 Completed - Clinical trials for Coronary Heart Disease

A Clinical Trials of Quick-Acting Heart Reliever for Moderate Coronary Stenosis

Start date: April 2012
Phase: Phase 4
Study type: Interventional

This study investigates the effective power of angina pectoris after Quick-Acting Heart Reliever and isosorbide dinitrate interventing respectively the patients with moderate coronary stenosis for six months. At the same time, the studying will assess the plaque, myocardial blood-supplying,quality of life and observe the end point of the heart (including the myocardial revascularization, death and myocardial infarction). The purpose is to study the function of the blood-quickening stasis-transforming formula Quick-Acting Heart Reliever for moderate coronary stenosis lesions.

NCT ID: NCT01511120 Completed - Clinical trials for Coronary Heart Disease

The Effect on Fluid Balance After Cardiac Surgery After Use of Two Different Priming Protocols

Start date: November 2011
Phase: Phase 2
Study type: Interventional

"The impact on fluid loading after cardiac surgery by use of two different priming solution" Fluid overloading with oedema formation is a regular finding following on-pump cardiac surgery and may contribute to postoperative organ dysfunction. Myocardial oedema has been reported to impair both systolic and diastolic function. An association between intraoperative fluid loading and postoperative adverse outcome has been demonstrated in cardiac patients. The investigators have experience with the use of both colloides and combination fluids (hypertonic saline/colloides) in several experimental studies (pigs). In one animal study the investigators used colloides as an additive to the CPB-prime. The investigators observed reduced fluid leakage and less total tissue water in several organs. The planned study includes patients scheduled for coronary artery bypass, and who have no co-morbidity. The patients will be randomized to receive either Tetraspan® (HES) or acetated Ringer`s solution in the CPB-prime. Accurate accounts of fluid additions, blood loss and diuresis will be kept. Determination of cardiac output (C.O.), intrathoracic blood volume (ITBV), extravascular lung water (EVLW) and global end diastolic volume (GEDV) will be monitored by use of the transpulmonary thermodilution technique PiCCO®plus system.