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Coronary Artery Disease clinical trials

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NCT ID: NCT01700972 Withdrawn - Clinical trials for Coronary Artery Disease

Feasibility and Diagnostic Accuracy of Myocardial Perfusion Imaging Using Early Imaging Protocol

Start date: February 2013
Phase: Phase 4
Study type: Interventional

The current protocol for myocardial perfusion imaging (MPI) entails imaging within 30-45 minutes after radiotracer injection, for both rest and stress studies. We hypothesize that early imaging 10 minutes after radiotracer injection provides high image quality and diagnostic accuracy comparable to 30-45 minutes MPI.

NCT ID: NCT01681524 Withdrawn - Clinical trials for Coronary Artery Disease

Open Label Study to Access Flurpiridaz F18 in PET MPI Verses SPECT MPI

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

The study will evaluate the use of Flurpiridaz F18 injection in patients with CAD to determine if the study drug in PET imaging is better than SPECT imaging currently used for this purpose.

NCT ID: NCT01655524 Withdrawn - Clinical trials for Coronary Artery Disease

The Impact of the Routine Aminophylline Administration Following Regadenoson Stress on SPECT Myocardial Perfusion

ASSUAGE-MPI
Start date: July 2012
Phase: Phase 4
Study type: Interventional

The investigators developed a modified regadenoson nuclear stress test of the heart that incorporates an aminophylline injection following regadenoson (The ASSUAGE protocol). The modified (ASSUAGE) protocol has been associated with fewer side effects and was better tolerated by patients. This study will investigate whether the modified regadenoson stress protocol (ASSUAGE) produces blood flow pattern to the heart similar to that of a standard regadenoson stress protocol. In proven to be the case, the ASSUAGE protocol has the potential to be used on a wide scale instead of the current standard protocol.

NCT ID: NCT01631409 Withdrawn - Clinical trials for Coronary Heart Disease (CHD)

Estimation of the Long Term Effectiveness of Routine Use of Cardiac Shock Wave Therapy

CSWTSPB40
Start date: September 2013
Phase: N/A
Study type: Observational

This study is dedicated to determination of the long term effectiveness of coronary heart disease (CHD) treatments - cardiac shock wave therapy (CSWT) in comparison with other kinds of medical and surgical treatment. For that purpose the investigators will observe the patients with CHD who enrolled in this study in their routine course of treatment. But the investigators will not interfere with the patient treatment. Each participant will be followed-up for five years. The collected data will allow to determine if the particular method, CSWT, could really make any additional contribution to the more traditional methods of CHD treatment and if the CSWT is only temporarily effective or could exert the long term effect as well.

NCT ID: NCT01622387 Withdrawn - Clinical trials for Coronary Artery Disease

Radial Artery Versus Saphenous Vein Patency (RSVP) Trial - 10 Year Follow-up

Start date: October 13, 2011
Phase: N/A
Study type: Interventional

During coronary bypass surgery, veins are taken from the leg and applied to the heart and aorta to 'bypass' narrowings in the coronary arteries. However using an artery in the chest, the internal mammary artery, means that the bypass lasts longer than using veins. The investigators recently showed that using an artery from the arm as a bypass vessel, the radial artery, also had less furring up than veins 5 years after surgery. Now the investigators would like to ask patients to come back for an angiogram 10 years following surgery.

NCT ID: NCT01620320 Withdrawn - Stenosis Clinical Trials

Stress Echocardiography Versus Coronary Angiography for Left Main Stenosis Detection

ESTRIE-TC
Start date: July 2010
Phase: N/A
Study type: Observational

Left main stenosis use to be treated by bypass but with the improvement of angioplasty techniques, an increasing number of patients are submit to left main coronary angioplasty. Consequences of left main intra stent stenosis can be disastrous yet, for the moment, no precise recommendation concerning the follow up of these patients exist. The investigators ought to determine if stress echocardiography can predict left main intra stent stenosis as well (non inferiorly)as control angiography that use to be done.

NCT ID: NCT01612299 Withdrawn - Renal Transplant Clinical Trials

Effects of Zortress® + Tacrolimus vs. Standard Immunosuppression on Progression of Coronary Artery Calcifications and Bone Disease in de Novo Renal Transplant Recipients

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

Primary objectives: A. To evaluate the effect of Zortress® versus standard immunosuppression therapy on progression of CAC as evidenced by changes in Agatston scores from baseline and at 6, and 12 months in renal transplantation patients. B. To investigate progression of CAC in patients undergoing renal transplantation within the study period. Secondary objectives: 1. To evaluate in renal transplantation the effect of Zortress® versus standard immunosuppression therapy on bone mass as evidenced by changes in quantitative computed tomography (QCT) and dual energy X-ray absorptiometry (DXA). 2. To evaluate in renal transplantation the effect of Zortress® versus standard immunosuppression therapy on activity of bone forming and resorbing cells as evidenced by changes in bone histology. 3. To evaluate in renal transplantation the effect of Zortress® versus standard immunosuppression therapy on biochemical parameters of bone turnover as evidenced by changes in serum Parathyroid Hormone (PTH), Bone-Specific Alkaline Phosphatase (BSAP), Tartrate-Resistant Acid Phosphatase (TRAP), Sclerostin, Receptor Activator of Nuclear factor Kappa B Ligand (RANKL), Osteoprotegerin (OPG), , serum CTX (C-terminal telopeptide of type 1 collagen), and urinary NTX (N-terminal cross link telopeptide). 4. To evaluate in renal transplantation the effect of Zortress® versus standard immunosuppression therapy on cardiovascular events, graft rejection and patient survival.

NCT ID: NCT01584622 Withdrawn - Clinical trials for Coronary Artery Disease

Clinical Evaluation of the CADenceTM System in Detection of Coronary Artery Diseases

CADENCE
Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the effectiveness of the CADence system, a non-invasive device, in detecting greater than or equal to 50% coronary stenosis anywhere in the coronary tree.

NCT ID: NCT01546870 Withdrawn - Clinical trials for Transplant Coronary Artery Disease

Coronary Artery Study in Pediatric Heart Transplantation

CAS-POHT
Start date: April 2012
Phase: N/A
Study type: Observational

Transplant coronary artery disease (TCAD) is a significant cause of morbidity and mortality in pediatric heart transplantation (PHT). Understanding the pathophysiology and early detection along with attempted medical management are crucial in preventing advancement of the disease and retransplantation or mortality. Coronary angiogram, although routinely used is insensitive to detect early TCAD. Measurement of fractional flow reserve (FFR), coronary flow reserve (CFR) and index of microvascular resistance (IMR) using a doppler pressure and flow intracoronary wire may be more sensitive in evaluating the integrity of coronary vasculature and thus detect pre clinical TCAD. To the best of the investigators knowledge, measurement of these parameters has not been previously reported in PHT.

NCT ID: NCT01411462 Withdrawn - Clinical trials for Coronary Artery Disease

VIBE-assisted DEB Registry

VIBER
Start date: August 2011
Phase:
Study type: Observational

VIBER aims at assessing angiographic outcome of drug-eluting balloon angioplasty assisted by the Vascular Imaging Balloon Catheter (VIBE, Volcano, San Diego, CA) device, which integrates a predilation catheter with electronic intravascular ultrasound capabilities.