Clinical Trials Logo

Atrial Fibrillation, Persistent clinical trials

View clinical trials related to Atrial Fibrillation, Persistent.

Filter by:

NCT ID: NCT04542785 Recruiting - Atrial Fibrillation Clinical Trials

Lenient Rate Control Versus Strict Rate Control for Atrial Fibrillation. The Danish Atrial Fibrillation Randomised Clinical Trial

DanAF
Start date: March 31, 2021
Phase: N/A
Study type: Interventional

Atrial fibrillation is the most common heart arrhythmia with a prevalence of approximately 2% in the western world. Atrial fibrillation is associated with an increased risk of death and morbidity. The comparable effects of a lenient rate control strategy and a strict rate control strategy in patients with atrial fibrillation are uncertain and only one trial has assessed this previously in patients with permanent atrial fibrillation. The investigators will therefore undertake a randomised, superiority trial at four hospitals in Denmark.

NCT ID: NCT04508491 Enrolling by invitation - Cognitive Function Clinical Trials

Cognitive Function in Patients With Persisted Atrial Fibrillation

SMART-AF
Start date: November 30, 2020
Phase: N/A
Study type: Interventional

Compare the difference of cognitive function between different treatment strategy in patients with persistent atrial fibrillation

NCT ID: NCT04500184 Completed - Clinical trials for Cardiac Rehabilitation

Exercise-based Cardiac Rehabilitation After Thoracoscopic Ablation in Patients With Persisent Atrial Fibrillation

Start date: June 1, 2017
Phase:
Study type: Observational

Thoracoscopic ablation is a promising treatment of persistent atrial fibrillation. However, the postoperative rehabilitation is very important to prevent early recurrence of atrial arrhythmia. The purpose of this study is to evaluate the efficacy of professional cardiac rehabilitation in patients after thoracoscopic ablation.

NCT ID: NCT04489004 Completed - Clinical trials for Atrial Fibrillation, Persistent

The Chinese Registration Study of Driver Ablation of Persistent Atrial Fibrillation.

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

This is an open label, multi-center, randomized parallel control clinical trial, to demonstrate the role of driver mechanism in maintenance substrate of persistent atrial fibrillation, and evaluate the clinical outcomes of driver mapping and ablation strategy in patients with persistent atrial fibrillation.

NCT ID: NCT04473963 Completed - Clinical trials for Atrial Fibrillation, Persistent

FLOW-AF: A Study to Evaluate the Ablacon Electrographic FLOW EGF Technology

FLOW-AF
Start date: September 27, 2019
Phase: N/A
Study type: Interventional

This study is to evaluate the Ablacon Electrographic Flow (EGF) algorithm technology (Ablamap Software).

NCT ID: NCT04342312 Recruiting - Atrial Fibrillation Clinical Trials

Intensive Molecular and Electropathological Characterization of Patients Undergoing Atrial Fibrillation Ablation

ISOLATION
Start date: March 5, 2020
Phase:
Study type: Observational

Rationale: Although there are several individual factors which are known to influence the chances of successful atrial fibrillation (AF) ablation, it remains a challenge to identify patients at risk for ablation failure with satisfactory certainty. Objectives: To identify predictors of success of AF ablation including clinical factors, AF recurrence patterns, anatomical and electrophysiological characteristics, circulating biomarkers and individual genetic background. Study design: Prospective registry of patients undergoing AF ablation. Clinical characteristics and results of routine tests are collected. In addition, the following (non-standard) tests are performed: extended surface electrocardiogram (extECG), extended rhythm monitoring, biomarker testing, genetic analysis, questionnaires. In subgroups of patients transesophageal electrocardiogram (TE-ECG), epicardial electroanatomical mapping and/or left atrial appendage (LAA) biopsy is performed. Study population: Patients aged 18 years and older with documented AF, scheduled for AF ablation. Main study endpoints: Ablation success after 12 and 24 months, defined as freedom from any episode of documented atrial arrhythmia after the blanking period.

NCT ID: NCT04237389 Recruiting - Clinical trials for Atrial Fibrillation, Persistent

Thoracoscopic Ablation Versus Catheter Ablation in Patients With Atrial Fibrillation

TACAAF
Start date: March 22, 2019
Phase: N/A
Study type: Interventional

Despite good progress in the management of patients with atrial fibrillation (AF), this arrhythmia remains one of the major causes of stroke, heart failure, sudden death, and cardiovascular morbidity in the world. Furthermore, the number of patients with AF is predicted to rise steply in the coming years. Even if the amount of antiarrhythmic drugs (AAD) is constantly increasing, there is a group of patients who has AF, resistant to AAD therapy. In such cases they are being offered alternative minimally invasive procedures, such as catheter or thoracoscopic ablation. With the discovery that AF often is initiated and maintained by electrical instability inside and around the pulmonary veins (PV) catheter and thoracoscopic ablation are now widely accepted invasive strategies to cure AF. Even though the results of both of the procedures are very promising in treating patients with paroxysmal AF, the decision making process, which approach should be used in patients with persistant or LSPAF, is still very controversial. According to 2016 ESC Guidelines for the management of atrial fibrillation developed in collaboration with EACTS, catheter or surgical ablation should be considered in patients with symptomatic persistent or long-standing persistent (LSP) AF refractory to AAD therapy to improve symptoms, considering patient choice, benefit and risk, supported by an AF Heart Team (IIaC). Since, there is no actual evidence base, which approach is more effective and save in patients with persistant and LSP AF, the aim of the investigator's study is to evaluate the results of both of the approaches in such group of patients.

NCT ID: NCT04229160 Recruiting - Clinical trials for Atrial Fibrillation, Persistent

Noninvasive 3D Mapping in Persistent Atrial Fibrillation, to Describe Modifications of the Arrhythmogenic Substrate After Pulmonary Vein Isolation and Identify Potential Predicting Factors of Ablation Success

CRYOVEST
Start date: June 9, 2020
Phase: N/A
Study type: Interventional

Atrial fibrillation (AF) is the most common cardiac arrhythmia in adults. It is a major cause of ischemic stroke and heart failure. Intravascular cardiac ablation of the left atrium by catheter delivery is an efficient treatment to restore sinus rhythm. AF ablation is a class IIa treatment for patients with symptomatic persistent AF refractory or intolerant to antiarrhythmic medication. There are still many debates considering the ablation strategy. The pulmonary veins remain the cornerstone of AF ablation therapy, even in persistent AF. There is a large electrical remodeling occurring in the left atrium between paroxysmal AF, early persistent AF and long-standing persistent AF. However, no multicentric and randomized study has demonstrated so far the interest of targeting other left atrial substrate, such as rotors or focal sources. Our study aims to describe with a noninvasive mapping system the arrhythmogenic substrate of persistent AF > 6 months pre- and post-cardioversion, and after pulmonary vein isolation.

NCT ID: NCT04206917 Terminated - Atrial Fibrillation Clinical Trials

MultiPulse Therapy (MPT) for AF

Start date: March 19, 2020
Phase: N/A
Study type: Interventional

Assess the clinical safety and feasibility of MultiPulse Therapy (MPT) electrical stimulation waveform sequence in terminating paroxysmal and persistent atrial fibrillation.

NCT ID: NCT04148664 Completed - Atrial Fibrillation Clinical Trials

A Trial of High Power-Short Duration Versus Standard Power-Long Duration Radiofrequency Ablation for Treatment of Atrial Fibrillation

Short-AF
Start date: December 3, 2019
Phase: N/A
Study type: Interventional

This study is a prospective, randomized controlled study to compare overall clinical outcomes between High Power Short Duration (HPSD) and standard radiofrequency (RF) ablation settings for Atrial Fibrillation (AF) ablation in the treatment of subjects with paroxysmal or persistent Atrial Fibrillation.