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Coronary Disease clinical trials

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NCT ID: NCT01838148 Recruiting - Clinical trials for Coronary Artery Disease

Biochemical and Electrocardiographic Signatures in the Detection of Exercise-induced Myocardial Ischemia

BASEL VIII
Start date: May 2004
Phase:
Study type: Observational

The primary aim is to perform the largest study worldwide to evaluate novel biochemical and electrocardiographic signatures alone as well as in combination with the standard 12-lead exercise ECG in the detection of exercise-induced myocardial ischemia (diagnostic endpoint). The secondary aim is to evaluate these innovative tools in the risk prediction for the occurrence of cardiovascular death and acute myocardial infarction during long-term follow-up.

NCT ID: NCT01825759 Recruiting - Clinical trials for Coronary Heart Disease

Danshen Dropping Pill for Coronary Heart Disease Heart and Artery Structure and Function

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

The Impact of Compound danshen dropping pill for coronary heart disease (CHD) heart and artery structure and function in patients with hypertension

NCT ID: NCT01823185 Recruiting - Clinical trials for Coronary Artery Disease

Bedside Testing of CYP2C19 Gene for Treatment of Patients With PCI With Antiplatelet Therapy

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

Clopidogrel is crucial as antiplatelet treatment in patients undergoing percutaneous coronary intervention (PCI) with stent implantation and during one year after PCI, to prevent atherothrombotic complications. However, clopidogrel is ineffective in certain patients due to genetic mutation in CYP2C19 gene a specific enzyme in the liver required for metabolism of clopidogrel. Therefore, the purpose of this study is to test these patients genetically at bedside and prescribe an alternative drug such as Ticagrelor (90 mg twice daily) or prasugrel ( 10mg once daily or 5mg once daily if the patient older than 75 years or a body weight < 60kg) if they are carriers of the allele 2 or 3 of the mutated gene.

NCT ID: NCT01810224 Recruiting - Clinical trials for Coronary Artery Disease

Graft Patency After FFR-guided Versus Angio-guided CABG (GRAFFITI) Trial

GRAFFITI
Start date: March 2013
Phase: Phase 4
Study type: Interventional

This is prospective, randomized, multicenter, multinational, randomized (1:1) study. The aim of this study is to assess the importance of functional assessment of coronary artery disease prior to bypass surgery. In particular, an FFR-guided strategy will be compared to the traditional Angio-guided strategy in the guidance of surgical revascularization by aorto-coronary bypass grafting.

NCT ID: NCT01796873 Recruiting - Clinical trials for Coronary Artery Disease

Clopidogrel Resistance and Platelet Reactivity in Women Undergoing Percutaneous Coronary Intervention

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

Plavix (clopidogrel) is a drug that is approved by the FDA (Food and Drug Administration) to reduce the risk of having another heart attack by preventing platelets (blood cells that are important in forming blood clots) from sticking together and forming another clot. Platelet activity can be measured by a machine called VerifyNow. The purpose of this study is to see whether Hispanic women and White non-Hispanic women have the same platelet response to a commonly used drug, Plavix (clopidogrel). Recent studies have shown that platelets may be more active in Hispanics, making it more difficult to prevent clots from forming, even when using Plavix. In addition, studies have shown that women may also have more active platelets than men. There have been no studies of Hispanic women and the effect of Plavix on platelet activity.

NCT ID: NCT01788592 Recruiting - Clinical trials for Coronary Artery Disease

Prospective Evaluation of Drug-Eluting Stents in Routine Clinical Practice (ASAN PCI Registry)

Start date: January 2003
Phase:
Study type: Observational [Patient Registry]

The objective of this study is to evaluate effectiveness and safety of drug-eluting stent implantation in the "real world" daily practice.

NCT ID: NCT01781715 Recruiting - Clinical trials for ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease

Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting Stent for STEMI

ZES for STEMI
Start date: September 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine outcomes (death, myocardial infarction, target vessel revascularization (TVR), non-target vessel revascularization (non-TVR), stent-thrombosis) of 120 consecutive patients with ST elevation myocardial infarction and multivessel coronary artery disease undergoing multivessel stenting or staged percutaneous coronary intervention with Zotarolimus-eluting stents

NCT ID: NCT01779986 Recruiting - Clinical trials for Coronary Artery Disease

Comparison of the Evaluation of CAD by CT AngioScan and Coronary Angiogram

CTAS-MCAS
Start date: January 2013
Phase: N/A
Study type: Observational

The use of CT Coronary Angioscan (CT-AS) is gaining popularity, but its exact value as evaluation of CAD requires confirmation. We intend to compare the results of CT-AS and convention coronary angiogram results in patients who are scheduled for an ascending aorta aneurysm reparation surgery. These examens are standard of care before this surgery, so there is no additional danger or disadvantage for the patient. We hope to confirm that CT-AS is a reliable screening test for CAD in patient undergoing heart surgery for other reason than CAD.

NCT ID: NCT01776567 Recruiting - Clinical trials for Coronary Artery Disease

Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluting Everolimus From Cobalt Versus Platinum Alloy Platforms

APPOSE
Start date: July 2012
Phase: Phase 4
Study type: Interventional

The purpose of the trial is to directly compare the Cobalt Chromium platform everolimus-eluting stent, Xience Primeâ„¢, with the Platinum Chromium platform everolimus-eluting stent, Promus Elementâ„¢, in relation to stent scaffolding shape, position with the heart blood vessel and extent of tissue coverage (at 6 months) using optical coherence tomography. Hypotheses: 1. The alloy composition and strut design of a drug-eluting stent has a direct bearing on stent apposition measured using OCT. 2. Stent design and alloy composition have a direct influence on radial support and scaffold shrinkage.

NCT ID: NCT01773512 Recruiting - Clinical trials for Coronary Artery Disease

The Prediction of Extent and Risk Profile of Coronary Atherosclerosis and Their Changes During Lipid-lowering Therapy Based on Non-invasive Techniques

PREDICT
Start date: June 2012
Phase: Phase 4
Study type: Interventional

- The prediction of extent and risk profile of coronary atherosclerosis based on clinical evaluation and non-invasive techniques. - Detailed analysis of plaque volume, plaque composition, risk plaque features and shear stress (WSS) changes during lipid lowering therapy (rosuvastatin 40mg) from 3D vessel reconstruction. - Prediction of changes in coronary arteries based on changes in non-invasive examinations. - Examination of WSS influence on atherosclerosis development and changes of WSS during lipid lowering therapy.