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Stable Angina Pectoris clinical trials

View clinical trials related to Stable Angina Pectoris.

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NCT ID: NCT00825604 Withdrawn - Clinical trials for Stable Angina Pectoris

Quality of Life and Target Achievement After Treatment of Patients With Stable Angina Pectoris

LOBSTR
Start date: January 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to, in patients with stable angina pectoris, assess the additional benefit of PCI on top of optimized medical treatment, physical training and smoking cessation with regard to quality of life, achievement of target of treatment and clinical events such as death, acute myocardial infarction, stroke and revascularization.

NCT ID: NCT00763464 Completed - Clinical trials for Stable Angina Pectoris

Coronary Artery Disease (CAD) in Postmenopausal Women

FEMCAD
Start date: October 2006
Phase: N/A
Study type: Interventional

Aim of this study is the determination of a valid procedure for ischemia diagnositc in postmenopausal women.

NCT ID: NCT00638326 Terminated - Clinical trials for Stable Angina Pectoris

Doubling the Maintenance Dose of Clopidogrel in Patients With High On-Clopidogrel Platelet Reactivity

DOSER
Start date: March 2008
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine whether administration of 150 mg clopidogrel is effective in reducing the one-year incidence of thromboischemic events in patients with high on-clopidogrel platelet reactivity compared to 75 mg clopidogrel after elective percutaneous coronary intervention.

NCT ID: NCT00352014 Completed - Clinical trials for Stable Angina Pectoris

Evaluation and Comparison of Several Point-of-care Platelet Function Tests in Predicting Clinical Outcomes in Clopidogrel Pre-treated Patients Undergoing Elective PCI.

Start date: January 2006
Phase:
Study type: Observational

The purpose of this study is to investigate whether the level of Platelet Inhibition as assessed with five point-of-care platelet function assays correlates with clinical (periprocedural) outcomes such as Acute Myocardial Infarction, death, Target Vessel revascularization and/or stroke in patients undergoing elective PCI.

NCT ID: NCT00281346 Completed - Clinical trials for Acute Myocardial Infarction

Non-invasive Diagnosis of Coronary Artery Stenoses by Doppler Echocardiography

Start date: December 2005
Phase: N/A
Study type: Interventional

Non-invasive evaluation of patients with stable angina and unstable coronary syndromes with transthoracic Doppler echocardiography to evaluate presence of significant coronary stenoses. Blinded evaluation and comparison with coronary angiography: presence and location of stenoses, and head to head comparison of clinical value and patient classification.

NCT ID: NCT00176358 Recruiting - Clinical trials for Stable Angina Pectoris

Percutaneous Coronary Angioplasty Compared With Exercise Training in Symptomatic Coronary Artery Disease

Start date: n/a
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to compare coronary angioplasty with stent implantation with an exercise rehabilitation program in patients with stable coronary artery disease (CAD).

NCT ID: NCT00157001 Terminated - Clinical trials for Stable Angina Pectoris

Feasibility Study of Photopheresis Post Angioplasty

Start date: August 2000
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to evaluate the difference in 6-month restenosis rates in coronary artery lesions treated by photopheresis in addition to angioplasty with stent placement, as opposed to no photopheresis after angioplasty and stent placement. Restenosis means the closing up again, or narrowing in diameter, of the previously treated artery, which may cause reduced blood flow and the re-occurrence of symptoms. Photopheresis is a therapeutic technique in which a portion of your white blood cells is collected by a blood separation device and exposed to ultraviolet A light, in combination with the drug 8-MOP (8-methoxypsoralen), then returned to you. The secondary objectives are: 1. To compare the incidence of major adverse cardiac events (MACE) between the three treatment groups for 6 months post-angioplasty. MACE events include death (cardiac related), myocardial infarction, coronary artery bypass graft surgery, repeat angioplasty to the target vessel, hospitalization and clinical symptoms. 2. To evaluate the safety of the treatment by comparing the incidence of acute and subacute thrombosis, bleeding and vascular complications and other non-MACE events every 2 weeks for 6 months post-angioplasty between the three treatment groups.