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Coronary Disease clinical trials

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NCT ID: NCT01789814 Completed - Clinical trials for Coronary Artery Disease

Effect of Prasugrel Versus Clopidogrel on Platelet Function After Bivalirudin Cessation

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

Early stent thrombosis has been noted with increased frequency in acute coronary syndrome (ACS) patients undergoing percutaneous coronary intervention (PCI) who are treated with bivalirudin and clopidogrel. The brief half life of bivalirudin acting in concert with the delayed action of clopidogrel likely exposes patients to thrombosis during a vulnerable period of reduced antiplatelet effect in the immediate post stenting period. Combination therapy with bivalirudin and prasugrel is conceptually attractive as the more rapid onset of action of prasugrel could potentially significantly diminish the vulnerable period, likely reducing the potential for acute stent thrombosis. The trials which have documented the efficacy of prasugrel as compared to clopidogrel have, in general, not reported on patients in whom bivalirudin was utilized. Currently, in the United States, bivalirudin is the most commonly used adjunctive agent used during PCI. Using light transmission aggregometry, this study will examine the inhibition of platelet aggregation in patients randomized to treatment with clopidogrel vs prasugrel during the vulnerable period following the discontinuation of bivalirudin therapy. The investigators anticipate that this study will document significant enhancement of inhibition of platelet aggregation in patients randomized to prasugrel treatment.

NCT ID: NCT01787370 Completed - Clinical trials for Coronary Artery Disease

Mainz Registry of Flow-mediated Constriction

Start date: September 2009
Phase: N/A
Study type: Observational [Patient Registry]

The goal of the flow-mediated constriction/ FMC-registry is to investigate whether the measurement of endothelial function using flow-mediated dilation and flow-mediated constriction provides on the presence of coronary atherosclerosis and on the prognosis of patients undergoing coronary angiography.

NCT ID: NCT01785589 Completed - Clinical trials for Coronary Artery Disease

Validation of Myocardial Perfusion Imaging

CameraCZT
Start date: May 2012
Phase: Phase 4
Study type: Interventional

The new cadmium-zinc-telluride (CZT) technology is a powerful tool for cardiac nuclear medicine. The increased photon counting sensitivity of camera can be used to explore novel protocols like dual isotope (rapid stress Tl-201/rest Tc-99m protocol for use with high-speed SPECT MPI). The use of dual isotope imaging is very interesting because this imaging combines the use of thallium-201 with technetium-99m agents permitting optimal image resolution and simultaneous assessment of viability, all with an exam duration of approximately 20 minutes. However, no study compares stress thallium-201/rest technetium-99m sequential dual isotope high-speed myocardial perfusion imaging versus invasive coronary angiography. The investigators report here the first validation of high-speed protocol with dual isotope for myocardial perfusion imaging using invasive coronary angiography as the standard of reference.

NCT ID: NCT01779401 Completed - Clinical trials for Coronary Heart Disease

Clopidogrel Response Evaluation and AnTi-Platelet InterVEntion in High Thrombotic Risk PCI Patients

CREATIVE
Start date: September 2012
Phase: N/A
Study type: Interventional

To identify the high-risk patients who might have in-stent thrombosis after PCI with thromboelastography and to head-to-head compare two intensified antiplatelet therapeutic strategies of double-dosage Clopidogrel and triple antiplatelet therapy with Cilostazol with the standard antiplatelet therapy.

NCT ID: NCT01778218 Completed - Clinical trials for Coronary Artery Disease

A Single Center Study to Establish the Imaging Protocol of 99mTc-EC-DG in Evaluating the Presence and Severity of Coronary Artery Disease (CAD)

Start date: January 2013
Phase: Phase 2
Study type: Interventional

This study will assess the safety and tolerability of the investigational radiolabeled imaging agent technetium-99m-labeled ethylenedicysteine-deoxyglucose (99mTc-EC-DG). Additionally, the study will determine the specific times to best image the heart using a SPECT camera with the investigational imaging agent and compare the images to those taken while undergoing the standard rest and exercise/regadenoson testing previously performed to detect the presence and severity of Coronary Artery Disease (CAD).

NCT ID: NCT01776866 Completed - Clinical trials for Coronary Artery Disease

Image Content Analysis of Dural-axis Rotational Versus Standard Coronary Angiography

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

The investigators hypothesized that dual-axis rotational coronary angiography was non-inferior to standard coronary angiography with respect to diagnosis of coronary artery disease.

NCT ID: NCT01771536 Completed - Stable Angina Clinical Trials

The PCI Choice Trial: a Pilot Randomized Trial of a Decision Aid for Patients With Stable Coronary Artery Disease

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

Despite several large clinical trials clearly establishing that coronary revascularization (i.e. percutaneous coronary intervention - PCI) does not prolong survival or prevent myocardial infarction (MI) for stable coronary artery disease (CAD), patients with stable angina continue to believe that PCI is performed to improve these outcomes. Additionally, recent concerns have emerged of overuse of PCI among patients with little or no angina. Thus there is a compelling need to share with patients the risks and benefits of PCI prior to treatment to reach an informed decision. This study is designed to answer the question of whether a decision aid can improve patient knowledge, decisional conflict and patient satisfaction with decision-making compared to usual care for the treatment of stable angina.

NCT ID: NCT01768403 Completed - Hypertension Clinical Trials

Centralised Pan-Algerian Survey on the Undertreatment of Hypercholesterolemia

CEPHEUS
Start date: September 2010
Phase: N/A
Study type: Observational

Centralized Pan-Algerian Survey on the undertreatment of hypercholesterolemia. The purpose of this study is to establish the proportion of patients on lipid-lowering pharmacological treatment reaching the LDL-C goals according to the Third Joint European Task Force guidelines in the survey population.

NCT ID: NCT01766466 Completed - Clinical trials for Coronary Artery Disease

Cangrelor Ticagrelor Transition Study

Start date: January 2013
Phase: Phase 2
Study type: Interventional

To demonstrate that patients treated with cangrelor can be directly switched to oral ticagrelor and that patients treated with ticagrelor can be switched to cangrelor without a significant decrease in the extent of inhibition of platelet aggregation.

NCT ID: NCT01766271 Completed - Clinical trials for Coronary Heart Disease Risk

GENErating Behavior Change, An Integrative Health Coaching and Genetic Risk Testing Pilot

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

The purpose of this 4 group (2x2) pilot randomized controlled trial is to test the feasibility and logistics of incorporating genetic risk information (9p21)into standard Coronary Heart Disease (CHD) risk counseling or health coaching intervention (or both) in primary care at 2 Duke Clinics.