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Angina, Stable clinical trials

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NCT ID: NCT00797953 Completed - Angina Pectoris Clinical Trials

Phase II Multi-Center Study of T89 to Treat Chronic Stable Angina

T89 phase 2
Start date: February 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the anti-angina effect and dose response of T89, a 2-herb botanical drug product, in patients with chronic stable angina pectoris in the United States.

NCT ID: NCT00786734 Withdrawn - Clinical trials for Percutaneous Coronary Intervention

Pitavastatin Pre-Treatment Study in Patient With Elective PCI for Stable Angina Pectoris (PIPA)

Start date: August 2008
Phase: Phase 4
Study type: Interventional

Patients who is scheduled elective PCI are randomized to pitavastatin 4mg daily or without pitavastatin for 5 -7days before the procedure. Creatine kinase-MB, troponin I, and myoglobin levels are measured at baseline and at 8 and 24 hours after the procedure(1st evaluation). After PCI, pitavastatin will be administered for additional 4 weeks(2nd evaluation).

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: NCT00751491 Unknown status - Clinical trials for Percutaneous Coronary Intervention

Clopidogrel Versus Adenosin in Non Urgent Percutaneous Coronary Intervention (PCI)

RACE
Start date: September 2008
Phase: Phase 3
Study type: Interventional

Percutaneous coronary intervention (PCI) is associated with up to 30% incidence of myonecrosis, as reflected by elevation of cardiac enzymes in a successful procedure. Apart from side-branch occlusion, intimal dissection and coronary spasm, a possible aetiology of myonecrosis after PCI might be distal embolization of atherogenic materials from plaque disruption causing obstruction of blood flow at capillary level resulting in micro-infarction. Recent studies have suggested that pretreatment with adenosine in the cath lab and Clopidogrel and statins greater than 6 hours before may be associated with a reduction in infarct size after reperfusion therapy for acute myocardial infarction. Whether pretreatment with adenosine decreases the incidence of myonecrosis in patients undergoing non-urgent PCI is not fully known. The investigators propose that adenosine-induced hyperaemia can potentially ameliorate the deleterious effects of distal embolization associated with non-urgent PCI through dilatation of the microvasculature. Mechanistically, this may reduce capillary obstruction by facilitating the throughput passage of embolized platelet thrombi out to the venous end of the coronary circulation, thereby reducing the incidence of post-PCI myonecrosis. In this prospective, randomized, open-label study, the investigators evaluated the incidence of myonecrosis after non-urgent PCI with a treatment with intracoronary adenosine compared with pretreatment of loading dose of Clopidogrel 300/600 mg >/< 6 hours.

NCT ID: NCT00738491 Terminated - Clinical trials for Coronary Heart Disease

Effects of Ambient Air Pollution Exposure in Patients With Stable Angina Pectoris During Normal Daily Activities

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

The purpose of this study is to identify whether exposure to ambient levels of air pollution during normal daily activities has a functional impact on patients with coronary heart disease

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: 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: 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).