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Angina, Unstable clinical trials

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NCT ID: NCT02235753 Terminated - Clinical trials for Acute Myocardial Infarction

High-intensity Exercise After Acute Cardiac Event (HITCARE)

HITCARE
Start date: December 2014
Phase: N/A
Study type: Interventional

Despite the well-known health benefits of physical exercise in the prevention of chronic diseases, less attention has been focused on the use of physical exercise as an essential part of good treatment for chronic disease. The aims of the study are to investigate the feasibility, medical effects, cost-effectiveness, and social perspectives of the individualized exercise-based rehabilitation [2 different high-intensity training (HIT) protocols combined with usual care (UC)] after acute coronary artery disease (CAD) event. The medical aim is to study mediating mechanisms of the physiological, biochemical and molecular effects of exercise training on the clinical outcomes. The aim of the health-economic evaluation is to assess the changes in the Health-Related Quality of Life (HRQL) and health care related costs for estimating the cost-effectiveness of HIT-based exercise rehabilitation. The purpose of the sociological analysis is to find out the social processes which make possible the emergence of the desired welfare effects.

NCT ID: NCT02037412 Terminated - Clinical trials for Acute Coronary Syndrome

Impact of Ticagrelor on the Endothelial Healing Following Drug-eluting Stent Implantation in the Patients With Acute Coronary Syndrome

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

The investigators hypothesized that ticagrelor may enhance endothelial healing after DES implantation by increasing adenosine concentrations by the inhibition of adenosine uptake into erythrocytes, compared to clopidogrel. Thus, the investigators will evaluate the extent of endothelialization (stent strut coverage) and neointimal hyperplasia (neointimal thickness) 3 months after DES implantation by optical coherence tomography (OCT)

NCT ID: NCT02000661 Terminated - Clinical trials for Acute Coronary Syndrome

Routine Versus Selective Use of FFR to Guide PCI

FFR-SELECT
Start date: January 2014
Phase: Phase 4
Study type: Interventional

Fractional flow reserve (FFR) is a test that can be performed at the time of heart catheterization. It measures the change in pressure across a narrowing in the heart artery during high flow situation, and provides reliable information about the functional severity of the narrowing. FFR measurements accurately predict whether a stent is needed, and is considered an excellent test before placement of stents to treat narrowed heart arteries. However, FFR is not used in every case because of the extra time needed and the associated device costs. Cardiac Services BC (an agency of Provincial Health Services Authority) is sponsoring this study to find out if FFR should be used in most cases (routine), rather than the current selective approach.

NCT ID: NCT01781546 Terminated - Clinical trials for Coronary Artery Disease

Drug-Eluting Balloon in Stable and Unstable Angina

DEBUT
Start date: May 22, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare DEB with BMS in CAD patients who are at high risk of bleeding and in whom the use of DES is therefore avoided. Our hypothesis is that PCI with DEB is non-inferior to BMS in the treatment of stable CAD or in ACS (UAP or NSTEMI) in patients at high risk of bleeding.

NCT ID: NCT01356992 Terminated - Unstable Angina Clinical Trials

Patients With High-risk Acute Coronary Syndrome Without ST-segment Elevation

VECOR
Start date: July 2012
Phase: Phase 3
Study type: Interventional

This non-inferiority study aims at comparing Versa® to the reference enoxaparin (Clexane®, Sanofi-Aventis) in patients with high-risk unstable angina and NSTEMI. The main justification is the search for scientific evidence to prove the Versa® effectiveness for this new therapeutic indication, since it is a product with potential for reducing costs, with effectiveness and safety comparable to the reference drug.

NCT ID: NCT01204320 Terminated - Unstable Angina Clinical Trials

A COMparison Between PAClitaxel-coated Balloon and pacliTaxel-eluting Stent in the Treatment of In-Stent Restenosis (COMPACT-ISR)

COMPACT-ISR
Start date: January 2008
Phase: Phase 4
Study type: Interventional

This is a multicentric randomized comparison between paclitaxel-coated balloon angioplasty or paclitaxel-eluting stent implantation in patients with stable or unstable angina with the evaluation of restenosis by Quantitative Coronary Analysis.

NCT ID: NCT01106612 Terminated - Clinical trials for Coronary Artery Disease

Study Comparing CT Scan and Stress Test in Patients With Known Coronary Artery Disease Hospitalized for Chest Pain

PROSPECT-CAD
Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether coronary artery CT scanning or nuclear stress testing is better at diagnosing chest pain patients with known coronary artery disease to select appropriate candidates for coronary catheterization and re-vascularization.

NCT ID: NCT01011647 Terminated - Clinical trials for Acute Myocardial Infarction

Prevalence of Sleep Disordered Breathing

Start date: November 2009
Phase: N/A
Study type: Observational

A novel technique in identifying unspecified sleep apnea has been developed. This technique uses signals typical acquired from a bedside monitor that is found in critical care environments. Those signals are then processed by a sleep analysis algorithm to provide an Apnoea Hypopnea Index (AHI) score. This study is intended to determine whether the prevalence of sleep disordered breathing identification among patients in a Coronary Care Unit (CCU) using this novel approach is significantly different than using routine techniques.

NCT ID: NCT00518245 Terminated - Unstable Angina Clinical Trials

Ischemia Driven Enoxaparin Therapy in ACS Presenting as Low Risk (IDEAL)

IDEAL
Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether enoxaparin (an anticoagulant) is effective in the treatment of patients presenting to the emergency room with chest pain and no electrocardiogram or bloodwork evidence of a heart attack, but with other high risk clinical features

NCT ID: NCT00435487 Terminated - Clinical trials for Myocardial Infarction

Dalteparin Versus Unfractionated Heparin In Patients With Acute Coronary Syndrome

Start date: June 2007
Phase: Phase 4
Study type: Interventional

To compare efficacy and safety of dalteparin compared to unfractionated heparin in patients of non ST elevation acute coronary syndromes who are planned to undergo coronary interventions (angioplasty or bypass surgery)