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Coronary Disease clinical trials

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NCT ID: NCT00829660 Completed - Clinical trials for Acute Coronary Syndrome

Acarbose Cardiovascular Evaluation Trial

ACE
Start date: February 17, 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether acarbose therapy can reduce cardiovascular-related morbidity and mortality in patients with impaired glucose tolerance (IGT) who have established coronary heart disease (CHD) or acute coronary syndrome (ACS). A secondary objective of the study is to determine if acarbose therapy can prevent or delay transition to type 2 diabetes mellitus (T2DM) in this patient population.

NCT ID: NCT00827411 Completed - Clinical trials for Coronary Artery Disease

Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a Common Antiplatelet Treatment for DES Implantation, and Interruption Versus Continuation of Double Antiplatelet Therapy

ARCTIC
Start date: January 2009
Phase: Phase 4
Study type: Interventional

Our first hypothesis is that dose adjustment of aspirin and clopidogrel based on biological monitoring reduces the rate of severe cardiovascular complications compared to a conventional strategy in patients scheduled for drug eluting stent implantation and followed up for one year. Our second hypothesis is that interruption of clopidogrel / Prasugrel after one year of a combined therapy of clopidogrel/Prasugrel and aspirin is associated with a higher rate of severe cardiovascular complications as compared with patients in whom aspirin and clopidogrel / Prasugrel is maintained during the subsequent 6 months of follow-up.

NCT ID: NCT00826280 Completed - Clinical trials for Coronary Artery Disease (CAD)

Caffeine's Effect on Regadenoson Administration With Single Photon Emission Computed Tomography (SPECT) Myocardial Perfusion Imaging (MPI)

Start date: March 24, 2009
Phase: Phase 3
Study type: Interventional

Observe whether the administration of caffeine prior to regadenoson will affect the interpretation of test results in subjects with coronary artery disease (CAD) undergoing SPECT MPI

NCT ID: NCT00825981 Completed - Coronary Disease Clinical Trials

Primary and Secondary Hemostasis in Elective Coronary Artery Bypass Graft Surgery

HEMOCOR
Start date: January 2009
Phase: N/A
Study type: Observational

Patients undergoing elective coronary artery bypass graft surgery (CABG) are treated with platelet inhibitors to reduce myocardial infarction and mortality.However, this can increase perioperative bleeding. A retrospective analysis of the data in our institution has revealed a significant increase in transfusion requirements after elective CABG since 5 years. The aim of our study is to observe if this increase in transfusion requirements is due to platelet inhibitors or due to other coagulation abnormalities resulting from other anticoagulants.

NCT ID: NCT00825279 Completed - Clinical trials for Coronary Artery Disease

A Trial Comparing a Paclitaxel Eluting Stent With Biodegradable Polymer Versus a Bare Metal Stent

EUCATAX
Start date: August 2007
Phase: Phase 4
Study type: Interventional

The success of stent implantation has led to the increasingly widespread use of them in the treatment of coronary artery disease (Sigwart, Serruys, Fischman)and although stent restenosis is still a limit for this therapeutic mode (Serruys, Rodriguez) the new generation of stents with improved coating materials and the development of polymers that release different kinds of drugs that prevent the activation and/or proliferation of smooth muscle cells (ultimate cause of restenosis) (Grube, Rodriguez). shows major improvements on this matter. The new generation of stents with biodegradable polymers and short time of drug release gives new advantages to this therapeutic, multiple studies and registries challenge this new devices (Taxus I and II, RAVEL, SIRIUS, ERACI II and III). For this reason the present study aims to compare a stainless steel stent with a drug eluting stent with coated of biodegradable polymer matrix hemoparin and paclitaxel.

NCT ID: NCT00824434 Completed - Clinical trials for Coronary Artery Disease

A Prospective, Multi-center Trial to Assess an Everolimus-Eluting Coronary Stent System (PROMUS Elementâ„¢)

PLATINUM QCA
Start date: March 2009
Phase: Phase 3
Study type: Interventional

Compile acute (30-day) clinical outcomes data and 9-month angiographic and intravascular ultrasound (IVUS) data for the PROMUS Elementâ„¢ Everolimus- Eluting Coronary Stent System in the treatment of patients with a single de novo atherosclerotic lesion

NCT ID: NCT00823212 Completed - Clinical trials for Coronary Artery Disease

The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions

PLATINUM
Start date: January 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of the PROMUS Elementâ„¢ Everolimus-Eluting Coronary Stent System for the treatment of patients with up to 2 de novo atherosclerotic coronary artery lesions. This clinical trial compares outcomes in patients treated with PROMUS Element to those in patients treated with a different everolimus-eluting coronary stent. The lesions are of average length in average-sized vessels ("workhorse"). A companion sub-trial evaluates outcomes in smaller vessels (SV) and another sub-trial evaluates outcomes in longer lesions (LL).

NCT ID: NCT00822666 Completed - Clinical trials for Coronary Artery Disease

Clopidogrel and Response Variability Investigation Study 2

CLOVIS2
Start date: October 2008
Phase: Phase 3
Study type: Interventional

To evaluate the role of the genetic variant 2C19*2 on the pharmacodynamic response as assessed by optical aggregometry and on the pharmacokinetic response as assessed by measuring active metabolites following an oral administration of a loading dose of 300/900mg of clopidogrel in patients with established coronary artery disease.

NCT ID: NCT00822536 Completed - Clinical trials for Coronary Artery Disease

Optimal Duration of Dual Antiplatelet Therapy After Drug-eluting Stent Implantation

OPTIDUAL
Start date: January 2009
Phase: Phase 4
Study type: Interventional

To compare treatment with aspirin alone versus the combined antiplatelet treatment aspirin and clopidogrel after 12 months of combined antiplatelet treatment following drug-eluting stent (DES) implantation.

NCT ID: NCT00819377 Completed - Clinical trials for Coronary Artery Disease

Milrinone Inhaled in Cardiac Surgery

Start date: February 2009
Phase: Phase 2
Study type: Interventional

Pulmonary hypertension is an important morbidity factor in patients having to undergo cardiac surgery with cardiopulmonary bypass (ECC). Milrinone used in inhalation, shows evidence of being a pulmonary vasodilator able to possibly contribute to the reduction of pressure on the pulmonary artery.