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Angina Pectoris clinical trials

View clinical trials related to Angina Pectoris.

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NCT ID: NCT01582165 Completed - Angina Pectoris Clinical Trials

Women With Chest Pain and no Significant Coronary Artery Stenosis; A Study on Microvascular Resistance

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

Female patients presenting with persistent chest pain despite no obstructive coronary artery disease have impaired prognosis. Stress tests are often positive or inconclusive. As much as 20% of women with chest pain and minimal angiographic CAD have evidence of myocardial ischemia, suggesting impaired coronary microcirculation. The index of microvascular resistance (IMR) is a method for indirectly investigating microvascular function in the cardiac catheterization laboratory. 66 female patients, age 30-70 years, with chest pain and "normal" or near normal coronary angiograms will be included. After coronary physiologic evaluation, patients will be randomized in a double blind study to rosuvastatin 20 mg/day or matching placebo tablets for altogether 6 months. The investigators hypothesize that: 1. A substantial number of women with chest pain and normal or minimal pathology on angiograms have microvascular dysfunction defined by a raised IMR. 2. Statins, based on its pleiotropic action will improve endothelial function and thereby IMR.

NCT ID: NCT01567644 Active, not recruiting - Clinical trials for Refractory Angina Pectoris

Extracorporeal Shockwave Therapy for the Treatment of Refractory Chronic Angina Pectoris

Start date: January 2008
Phase: Phase 1
Study type: Interventional

Low intensity shockwaves have been proven in animal studies to induce local growth of new blood vessels from existing ones. The hypothesis of this study is that shockwave therapy could improve the symptoms of patients with refractory angina not amenable to revascularization with angioplasty or bypass surgery.

NCT ID: NCT01567592 Suspended - Clinical trials for Refractory Angina Pectoris

Extracorporeal Shockwave Therapy for the Treatment of Chronic Angina Pectoris

Start date: March 2009
Phase: Phase 1
Study type: Interventional

Low intensity shockwaves have been proven in animal studies to induce local growth of new blood vessels from existing ones. The hypothesis of this study is that shockwave therapy could improve the symptoms of patients with refractory angina not amenable to revascularization with angioplasty or bypass surgery.

NCT ID: NCT01566175 Recruiting - Refractory Angina Clinical Trials

Use of the Neovasc Coronary Sinus Reducer System for the Treatment of Refractory Angina Pectoris in Patients With Ngina Class 3-4 Who Are Not Candidates for Revascularization

Reducer
Start date: August 30, 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to implant the Reducer in patients with the symptoms of refractory angina, that suffer from refractory angina who demonstrate reversible ischemia.

NCT ID: NCT01558830 Unknown status - Clinical trials for Coronary Artery Disease

Safety of Amiodarone and Ranolazine Together in Patients With Angina

SARA
Start date: January 2012
Phase: Phase 4
Study type: Interventional

Ranolazine is an effective and remarkably safe agent for the treatment of patients with chronic stable angina, but its inhibition of voltage gated potassium channels and electrocardiogram (EKG) corrected QT (QTc) prolongation properties have lead many to question its safety when combined with antiarrhythmic drugs. The investigators have proposed a study to determine the safety of ranolazine in patients with chronic stable angina who also take amiodarone. And are conducting a prospective single-center randomized single-blinded placebo controlled trial to run out of our large cardiology practice setting at Cardiovascular Consultants of Nevada. The hypothesis is that there will be no difference in the ventricular arrhythmia burden. The primary outcome will be the measurement of ventricular arrhythmia episodes on serial holter monitor and other serially acquired recordings (such as electrocardiogram, pacemaker or implantable defibrillator (ICD) data, and stress test data) over a three month trial period.

NCT ID: NCT01557855 Completed - Clinical trials for Coronary Artery Disease

Investigation of a Novel Gene Expression Test (ASGES or Corus CAD) for Diagnosis of Obstructive Coronary Artery Disease

REGISTRY-I
Start date: April 2012
Phase:
Study type: Observational

The objective of this study is to collect data on the commercial use of Corus CAD (Age/Sex/Gene Expression score - ASGES) blood test to evaluate the clinical referral patterns of Primary Care Physicians after receipt of their patients' Corus Score, and to better understand patient management patterns for clinicians ordering the test.

NCT ID: NCT01556126 Completed - Clinical trials for Acute Myocardial Infarction

Clinical Performance of CRE8 Drug Eluting Stent in All Comer Population

PARTICIPATE
Start date: February 2012
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate safety and efficacy performances of CRE8 Drug Eluting Stent, in patients comparable to the everyday's clinical practice population, with a specific focus on diabetics, that will be part of a pre-specified study subgroup.

NCT ID: NCT01552109 Completed - Stable Angina Clinical Trials

Stable Angina Observational Registry

STAR
Start date: January 2012
Phase: N/A
Study type: Observational

The purpose of this study is to describe the clinical profile and current status of the diagnosis and management of stable angina in India by non-interventional consulting physicians (CP) through a large multicenter observational registry.

NCT ID: NCT01550614 Terminated - Angina, Stable Clinical Trials

Efficacy and Safety of Ad5FGF-4 for Myocardial Ischemia in Patients With Stable Angina Due to Coronary Artery Disease

ASPIRE
Start date: March 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether a single intracoronary infusion of Ad5FGF-4, delivered during induced transient ischemia, is effective in improving myocardial perfusion, angina functional class, patient symptoms, and quality of life. Short-term (8 weeks) and long-term (12 month) safety of Ad5FGF-4 will also be evaluated. The primary endpoint is change in adenosine triphosphate (ATP) stress SPECT reperfusion defect size.

NCT ID: NCT01549977 Terminated - Angina Clinical Trials

Effect of Febuxostat Compared to Placebo on Exercise Tolerance in Participants With Chronic Stable Angina

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of febuxostat, once daily (QD), compared to placebo as an add on to stable anti-anginal therapy, on the total exercise time of participants with Chronic Stable Angina.