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Myocardial Ischemia clinical trials

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NCT ID: NCT01880879 Recruiting - Clinical trials for Coronary Artery Disease

A Prospective Multicenter Trial Evaluating Helios Biodegradable Polymer SES Safety and Effectiveness in CAD Treatment

Pro-HOPE
Start date: January 2013
Phase: Phase 4
Study type: Interventional

research topic:helios After registration of clinical research bidders:kinhely bio-tech Co.Ltd study design:A prospective single treatment group multicenter clinical study Number of patients:Included in the subjects of 800 cases Main research purpose:Evaluation of safety and effectiveness Mainly studies the finish:1 year target lesion of the failure Inclusion criteria : one:Gender not limited at the age of 18 to 80 two:myocardial ischemia or angina symptoms of coronary artery disease three:A narrow is less than 50% treated with stents four:Comply with the instructions five:Voluntarily signed the informed consent form exclusion criteria: one:Pregnant women two:cardiac shock three:Against a suppository medicines or allergies four:Participated in other test research in the first 6 months five:Within 6 months after PCI plans to accept non cardiac surgery six:Non-compliant patient Follow-up time:A month for 6 months and 9 months to 1 year to 2 years follow-up progress plan:All center within 6 months after start of complete into the group

NCT ID: NCT01869842 Recruiting - Clinical trials for Coronary Artery Disease

Randomized Controlled Study of the Traditional Percutaneous Coronary Intervention and Intervention Using Optical Coherence Tomography of Incomplete Stent Adhesion and Extent of the Formation of Neointima by Resolute Zotarolimus-eluting Stent Insertion

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

Optical coherence tomography (OCT) after the stent procedure to improve the adhesion and expansion, or incomplete uncovered struts attached to the main track. OCT in clinical areas by improving the parameters of the best stent will be useful. However, for better results for optical coherence tomography in percutaneous interventions have little useful data on the role. Randomized controlled study of the traditional percutaneous coronary intervention and intervention using optical coherence tomography.

NCT ID: NCT01869309 Recruiting - Clinical trials for Coronary Artery Disease

Overcoming High On-Treatment Platelet Reactivity (HPR) During Prasugrel Therapy With Ticagrelor

HEIGHTEN
Start date: January 2014
Phase: Phase 4
Study type: Interventional

The primary objective is to determine the pharmacodynamic effect of ticagrelor dosing (180mg LD/ 90mg BID) at 2, 4 hours and 14 days in stable Coronary artery disease (CAD) patients who exhibit high-on prasugrel platelet reactivity defined as Vasodilator Stimulated Phosphoprotein-Phosphorylation (VASP-P) >50%.

NCT ID: NCT01867801 Recruiting - Clinical trials for Coronary Artery Disease

Portuguese Registry on Interventional Cardiology

PRIC
Start date: January 2002
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this Registry is creating a database management that allows continuous monitoring characteristics, evolution, prognostic indicators and management of patients undergoing coronary angioplasty in Portuguese Hospitals, and identify the appropriateness of clinical and interventional practice recommendations for diagnosis and treatment of coronary disease and monitoring its evolution.

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: NCT01826929 Recruiting - Clinical trials for Ischemic Heart Disease

Effectiveness New Health Care Organization Model in Primary Care for Chronic Cardiovascular Disease Patients Based

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

The purpose of this study is to determine whether a multifactorial primary care intervention based on chronic models can improve the level of control and reduce the number of hospital admissions in patients with ischemic heart disease.

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: NCT01824030 Recruiting - Clinical trials for Ischemic Heart Disease

FFR or OCT Guidance to RevasculariZe Intermediate Coronary Stenosis Using Angioplasty

FORZA
Start date: April 2013
Phase: Phase 3
Study type: Interventional

Whether to revascularize patients with angiographically-intermediate coronary lesions (AICL) is a major clinical issue. Intravascular techniques (assessing either the anatomy or the functional effect of coronary stenoses) are routinely used to better characterize coronary lesions. Among these,fractional flow reserve (FFR) provides validated functional insights while optical coherence tomography (OCT) provides high resolution anatomic imaging. Both techniques may be applied to guide decisions regarding the opportunity to revascularize patients with AICL and to optimize the result of percutaneous coronary intervention (PCI). We aim to compare the clinical and the economical impact of FFR versus OCT guidance in the percutaneous management of patients with AICL.

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.