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Atrial Fibrillation clinical trials

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NCT ID: NCT02756429 Completed - Atrial Fibrillation Clinical Trials

Quantification of Endothelial Thrombogenicity in Patients With Atrial Fibrillation

REMI-2
Start date: February 2014
Phase: N/A
Study type: Interventional

Atrial fibrillation (AF) is the most common cardiac arrhythmia. Because of its major impact on the general morbidity and risk of stroke, AF is a great concern for public health. Several mechanisms, including endothelial dysfunction and inflammatory processes, have been postulated as predisposing factors for AF, as well as for stroke. Both clinical and experimental studies highlight inflammation as a predisposing factor for AF and its complications. Nevertheless, the source of high inflammatory proteins in patients with AF is still unknown. We hypothesized that multilevel intracardiac and extracardiac (left femoral vein, coronary sinus, left atrium, pulmonary vein) measurements of several inflammatory proteins (VEGF) would help assessing the extent and the source of inflammation in AF patients. The measurement of von Willebrand factor (vWF) levels in multiple vascular sites would also help to define the site of endothelial dysfunction and of production of this thrombogenic factor. Although AF is associated with an increased risk of stroke, the risk is not homogeneous. Permanent and persistent AF are associated with similar thromboembolic risk to that of paroxysmal AF.

NCT ID: NCT02754349 Completed - Atrial Fibrillation Clinical Trials

Validation Study of Pulse Wave Velocity and Augmentation Index in Atrial Fibrillation

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

This study aims to evaluate the reliability of measurements of arterial stiffness (pulse wave velocity (PWV), pulse wave contour analysis (PWA), central augmentation index (AIx) and pulse pressure (PP)) in atrial fibrillation (AF). For this purpose 30 AF patients scheduled for electrical cardioversion will be included. PWV and PWA measurements will be carried out before and after cardioversion.

NCT ID: NCT02754154 Completed - Atrial Fibrillation Clinical Trials

Real-World Comparative Observational Study in Non-Valvular Atrial Fibrillation Patients Using Oral Anticoagulants

Start date: December 31, 2014
Phase:
Study type: Observational

The purpose of this study is to compare the risk of major bleeding event among nonvalvular atrial fibrillation patients treated with warfarin, apixaban, dabigatran and rivaroxaban.

NCT ID: NCT02747498 Completed - Clinical trials for Recurred Atrial Fibrillation

Comparison of Circumferential Pulmonary Vein Isolation and Complex Pulmonary Vein Isolation Additional Linear Ablation for Recurred Atrial Fibrillation After Previous Catheter Ablation: Prospective Randomized Trial (RILI Trial)

Start date: January 1, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the clinical outcomes depending on catheter ablation strategy for repeat ablation procedure among the patients with recurred atrial fibrillation after de novo catheter ablation. After randomization, we will conduct circumferential pulmonary vein isolation alone in a group, and additional posterior box isolation in the other group. Non-pulmonary vein foci ablation will be done in all patients. We will compare clinical recurrence rate, complication rate, and procedure time, etc.

NCT ID: NCT02745236 Completed - Atrial Fibrillation Clinical Trials

The Effect of Nurse Practitioner Led-Care on Quality of Life in Patients With Atrial Fibrillation

Start date: July 31, 2016
Phase: N/A
Study type: Interventional

Atrial fibrillation (AF) is the most common heart rhythm disease characterized by an irregular heart rhythm of the top part (atria) of the heart. It may cause unpleasant symptoms as well as increases the person's risk of stroke and heart failure. With an ageing population, increasing rates of AF and limited access to specialists, new methods of care, like nurse practitioners (NP) need to be assessed to meet patient specific needs and provide sustainable care. The objective of the project is to evaluate the effect of Nurse Practitioner-led care in people with AF on their quality of life. The Canadian Healthcare system is overwhelmed, with increasing costs and wait times. Contributing to these issues, is AF is the most common arrhythmia accompanied with costly complications including stroke and heart failure. Currently family or emergency room physicians ask general cardiologists or specialized cardiologists, to provide care to patients with AF. Unfortunately, there is limited access to their services. NP's are nurses who have taken extra education at University to treat patients and prescribe medications. This research project involves an NP who has specialized training in AF patient management. By utilizing an NP to provide care for patients with AF, the investigators hope to improve patient's quality of life and satisfaction with care. This may also reduce complications of AF.

NCT ID: NCT02743520 Completed - Atrial Fibrillation Clinical Trials

Arrhythmia Detection In Obstructive Sleep Apnea (ADIOS)

ADIOS
Start date: March 6, 2017
Phase: N/A
Study type: Interventional

The purpose of this research study is to learn about arrhythmia detection in obstructive sleep apnea (OSA). For several years patients with OSA have an increased likelihood of having irregular heartbeats. This study will determine how often patients with OSA have irregular heartbeats. This study will also define which OSA patients are most likely to have irregular heartbeats. The participant is being asked to be in the study because the participant has been diagnosed with obstructive sleep apnea (OSA).

NCT ID: NCT02742545 Completed - Heart Failure Clinical Trials

Impact of MayoExpertAdvisor on Provider Adherence

MEA Research
Start date: April 2016
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of MayoExpertAdvisor (MEA), a knowledge delivery tool, to improve adherence to best practices for patients with hyperlipidemia, atrial fibrillation and heart failure. Half of the clinicians will receive MEA, while the other half will not receive MEA. The investigators hypothesize care teams with access to MEA will act upon recommendations at a higher rate than those care teams in the standard of care arm without access to MEA.

NCT ID: NCT02737215 Completed - Atrial Fibrillation Clinical Trials

Prevention of Atrial Fibrillation After Coronary Artery Bypass Grafting in Patients With Obstructive Sleep Apnea

PAFOS
Start date: May 2, 2016
Phase: N/A
Study type: Interventional

Background. Atrial fibrillation is one of the most common complications in the postoperative period of coronary artery bypass grafting (CABG) surgery and usually associated with increased length of hospital stay and higher hospital costs. Among the main mechanisms involved, excessive sympathetic activation, oxidative stress and inflammation are fundamental elements in the pathophysiology of obstructive sleep apnea. Objectives. To evaluate the effects of continuous positive airway pressure (CPAP) in reduction of atrial fibrillation after CABG in patients with obstructive sleep apnea. Methodological procedures: A multicenter randomized controlled study to compare the incidence of atrial fibrillation between the intervention group and the control group, both monitored seven days with Holter.

NCT ID: NCT02734875 Completed - Atrial Fibrillation Clinical Trials

Improving Quality of Care - Managing Atrial Fibrillation Through Care Teams and Health Information Technology

IQ-MATCH
Start date: May 2016
Phase: N/A
Study type: Interventional

This stepped wedge randomized intervention will apply machine learning algorithms in an electronic health record system to identify primary care patients with non-valvular atrial fibrillation (AF) who are at high risk of stroke and not on anticoagulation therapy. An Anticoagulant Management Service (AMS) will offer support to primary care providers regarding treatment for relevant patients (either warfarin and novel oral anticoagulants). This study seeks to: 1. increase the proportion of appropriately anticoagulated patients with AF, 2. understand the reasons for lack of anticoagulation, and 3. document the proportion of patients with AF who are appropriately not anticoagulated (e.g. patient refusal, contraindication).

NCT ID: NCT02734758 Completed - Stroke Clinical Trials

Markers of Atrial Fibrillation

Start date: August 2011
Phase:
Study type: Observational

This study will evaluate whether a gene marker can improve the identification of atrial fibrillation in patients with ischemic stroke, and evaluate whether the decision to anticoagulate could be improved by a marker of atrial fibrillation.