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Angina, Stable clinical trials

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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: NCT00737958 Completed - Clinical trials for Coronary Heart Disease

The Effects of Diesel Exhaust Inhalation On Exercise Capacity In Patients With Stable Angina Pectoris

Start date: August 2008
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether exposure to diesel exhaust (air pollution) has a functional impact on patients with stable angina pectoris.

NCT ID: NCT00719992 Completed - Stable Angina Clinical Trials

Diagnostic Value of HS-CRP in Stable Angina.

Start date: April 2006
Phase: N/A
Study type: Interventional

The aim of this study was to assess the amount of additive value of HS-CRP levels to a positive exercise tolerance test (ETT) in predicting coronary artery disease (CAD) using coronary angiography as the gold standard. The investigators concluded that HS-CRP can be used as a single predictor of coronary vessel involvement in patients with stable angina and positive ETT.

NCT ID: NCT00607217 Completed - Clinical trials for Myocardial Infarction

The Efficacy of Influenza Vaccination in Patients With Coronary Artery Diseases

Start date: January 2008
Phase: Phase 2/Phase 3
Study type: Interventional

This study wishes to understand: 1. whether vaccination against influenza in coronary artery disease (myocardial infarction and stable angina) patients is as effective as it is in healthy subjects; 2. whether vaccination really decreases the episodes of influenza infection in those coronary artery disease patients who receive the vaccine than those who do not.

NCT ID: NCT00607178 Completed - Clinical trials for Myocardial Infarction

The Efficacy of Influenza Vaccine in Reducing Cardiovascular Events in Patients With Coronary Artery Diseases

IVCAD
Start date: January 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Influenza vaccine reduces the cardiovascular events in post-myocardial infarction (MI) patients and in those with stable angina (SA).

NCT ID: NCT00602017 Completed - Hypertension Clinical Trials

Bioequivalency Study of Amlodipine Tablets Under Fasting Conditions

Start date: April 2004
Phase: N/A
Study type: Interventional

The objective of this study was the bioequivalence of a Roxane Laboratories' Amlodipine Besylate tablets, 10 mg, to Norvasc® Tablets, 10 mg (Pfizer) under fasting conditions using a single-dose, randomized, 2-treatment, 2-period, 2-sequence crossover design.

NCT ID: NCT00601302 Completed - Hypertension Clinical Trials

Bioequivalency Study of Amlodipine Tablets Under Fed Conditions

Start date: April 2004
Phase: N/A
Study type: Interventional

The objective of this study was the bioequivalence of a Roxane Laboratories' Amlodipine Besylate tablets, 10 mg, to Norvasc® Tablets, 10 mg (Pfizer) under fed conditions using a single-dose, randomized, 2-treatment, 2-period, 2-sequence crossover design.

NCT ID: NCT00474123 Completed - Stable Angina Clinical Trials

Antiplatelet and Anti-inflammatory Effects of Statins and Ezetimibe

Start date: January 2006
Phase: N/A
Study type: Interventional

Among patients with stable coronary artery disease (CAD), it is not clear if the pleiotropic effects of cholesterol reduction differ between high-dose simvastatin alone and combined ezetimibe/simvastatin. The investigators sought to compare the anti-inflammatory and anti-platelet effects of ezetimibe 10 mg / simvastatin 20 mg (E10/S20) to simvastatin 80 mg (S80).

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: NCT00346437 Completed - Angina Pectoris Clinical Trials

Efficacy and Safety of Intracoronary Ad5FGF-4 in Patients With Stable Angina (AGENT-3)

Start date: October 2001
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether a single intracoronary infusion of Ad5FGF-4 is effective in improving exercise capacity measured by exercise treadmill testing, angina functional class, patient symptoms, quality of life, and cardiovascular outcomes. Two doses will be studied, 2.87 x 10(8) and 2.87 x 10(9) viral particles, to evaluate the dose-response of Ad5FGF-4. Short-term and long-term safety of Ad5FGF-4 will also be evaluated.