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Angina Pectoris clinical trials

View clinical trials related to Angina Pectoris.

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NCT ID: NCT02845531 Recruiting - Clinical trials for Sudden Cardiac Death

Implantable Cardioverter Defibrillator Versus Optimal Medical Therapy In Patients With Variant Angina Manifesting as Aborted Sudden Cardiac Death

VARIANT ICD
Start date: November 29, 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether ICD(Implantable Cardioverter Defibrillator) implantation on the top of optimal medical therapy in patients with variant angina manifesting as aborted sudden cardiac death reduces the incidence of the death from any cause compared with optimal medical therapy alone.

NCT ID: NCT02773615 Recruiting - Angina Pectoris Clinical Trials

CT Perfusion Added to CT Angiography

PERFeCT
Start date: September 28, 2017
Phase:
Study type: Observational [Patient Registry]

Background In the differential diagnosis of unstable angina versus non-anginal chest pain, an exercise test is often the modality of choice for further investigation. However, in a substantial number of patients exercise testing is less informative, because of insufficient exercise capacity or pre-existing ECG-abnormalities. In patients with low pretest probability of coronary artery disease (CAD), Coronary CT angiography (CTA) has an excellent negative predictive value, but in patients with an intermediate or high pretest probability of CAD estimation of the hemodynamic significance of a stenosis has only limited specificity. CT perfusion (CTP) is a new method looking at myocardial perfusion during vasodilative stress with a sensitivity, specificity, positive predictive value and negative predictive value of respectively 81%, 93%, 87% and 88%, whereas radiation is limited to a maximum of 5 millisievert (mSv). Aim It is the aim of this pilot study to investigate whether the addition of CTP to CTA is a feasible and safe investigational workflow in patients with unstable angina or nonanginal chest pain in the emergency department.

NCT ID: NCT02760732 Recruiting - Angina, Unstable Clinical Trials

Drug Eluting Balloon for Treatment of Unstable Angina

Start date: November 2015
Phase: N/A
Study type: Interventional

This study was to investigate the effect and safety of drug eluting balloon combined for treatment of unstable angina.

NCT ID: NCT02623569 Recruiting - Angina Pectoris Clinical Trials

To Assess the Anti-anginal Safety and Efficacy of Ivabradine in Subjects With Stable,Symptomatic Chronic Angina

Start date: October 2014
Phase: Phase 2
Study type: Interventional

Arms Assigned Interventions Experimental: Ivabradine Ivabradine 5 mg twice a day for first 4 weeks and 7.5mg twice a day when positive ETT and HR>60times/min or negative ETT and HR>80times/min of subjects. Active Comparator: Atenolol Atenolol 12.5 mg twice a day for first 4 weeks and 25mg twice a day when positive ETT and heard rate>60times/min or negative ETT and HR >80times/min of subjects.

NCT ID: NCT02530021 Recruiting - Clinical trials for Ischemic Heart Disease

Heart Rate Variability (HRV) Testing Compared With Exercise Stress Test in Hospitalized Patients With Chest Pain

Start date: August 2015
Phase: N/A
Study type: Observational

There are many patients hospitalized for chest pain, which don't have high risk features that require invasive coronary angiography, but are considered intermediate risk and for which ischemic heart disease can not be excluded. The current management for these patients is to perform a non invasive test in order to classify their risk. Exercise ergometry is a commonly used non invasive test to detect ischemia. that test is non-invasive, and does not involve radiation or intra-venous contrast. The test is limited for many patients, because of un-ability to exercise, or because of non-interpetable Electro Cardio-Graphy (ECG). Heart rate variability is well known to be a marker of ischemic heart disease. Heart rate variability testing is a non-invasive ECG monitoring technique. The study design is to identify hospitalized patients who are candidates for non-invasive stress testing, and to monitor their heart rate variability for one hour prior to the stress test.

NCT ID: NCT02499250 Recruiting - Clinical trials for Refractory Angina Pectoris

Effect of Daily Remote Ischemic Conditioning on the Life Quality of Refractory Angina Pectoris Patients

D-RIC-RAP
Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose is to test whether daily ischemic conditioning of the arms over 30 days could reduce the frequency and severity of angina pectoris and improve the life quality of refractory angina pectoris patients.

NCT ID: NCT02448485 Recruiting - Heart Failure Clinical Trials

High-Sensitivity Troponin T Plasma Levels in Patients With Aortic Stenosis (Tyrolean Aortic Stenosis Study-2)

TASS-2
Start date: June 2015
Phase:
Study type: Observational

TASS-2 (Tyrolean Aortic Stenosis Study-2) aims to characterize the clinical value of minimally elevated troponin T plasma levels both in patients with asymptomatic and symtomatic aortic stenosis.

NCT ID: NCT02328898 Recruiting - Clinical trials for Acute Coronary Syndrome

Randomized "All-comer" Evaluation of a Permanent Polymer Resolute Integrity Stent Versus a Polymer Free Cre8 Stent

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

The study objective is to assess the safety and efficacy of the Permanent Polymer Zotarolimus-Eluting Stent Resolute Integrity™ to the Polymer Free Amphilimus-Eluting Stent Cre8™ compared in an all-comer patient population. 1 month of dual antiplatelet duration will be applied in stable angina pectoris patients. Myocardial infarction patient population will be treated with 12 months of dual antiplatelet therapy.

NCT ID: NCT02319083 Recruiting - Clinical trials for Coronary Artery Disease

Outcome After Coronary Artery Bypass Grafting

E-CABG
Start date: January 2015
Phase: N/A
Study type: Observational

The E-CABG registry is a multicenter, European registry collecting data on the preoperative characteristics, treatment strategies and outcome of patients undergoing isolated coronary artery bypass grafting (CABG).

NCT ID: NCT02180971 Recruiting - Vasospastic Angina Clinical Trials

Multidetector Coronary CT In Vasospastic Angina

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the extent of coronary vessel stenosis between coronary spasm-induced angina attacks (named vasospastic angina, VSA) patients and health volunteers by multi-detector computed tomography angiography (MDCTA), and to evaluate the diagnostic efficacy of MDCTA in patients with VSA.