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Atrial Fibrillation clinical trials

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NCT ID: NCT02169037 Recruiting - Atrial Fibrillation Clinical Trials

Substrate Versus Trigger Ablation for Paroxysmal Atrial Fibrillation

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

This is a prospective randomized study to assess the safety and efficacy of FIRM (Focal Impulse and Rotor Modulation)-guided ablation for the treatment of symptomatic atrial fibrillation (AF). The study hypothesis is that the efficacy of AF elimination at 1 year will be higher by ablating patient-specific AF-sustaining rotors and focal sources by Focal Impulse and Rotor Modulation (FIRM) compared to conventional ablation alone (wide-area PV isolation).

NCT ID: NCT02156765 Recruiting - Stroke Clinical Trials

China Atrial Fibrillation Screening in Acute Ischemic Stroke Patients

CRIST
Start date: October 2013
Phase: N/A
Study type: Observational [Patient Registry]

Three purpose of this study: 1. Increase diagnosis rate and formulate the flow of diagnosis and treatment of AF in ischemic stroke patients; 2. Evaluation on specificity and sensitivity of STAF score; 3. Analyze the pathogenesis of ischemic stroke and risk factors and establish clinical database and sample database of ischemic stroke.

NCT ID: NCT02147444 Recruiting - Clinical trials for Non-valvular Atrial Fibrillation

Evaluation of Effectiveness and Safety of Xa Inhibitor for the Prevention of Stroke And Systemic Embolism in a Nationwide Cohort of Japanese Patients Diagnosed as Non-valvular Atrial Fibrillation

EXPAND
Start date: November 2012
Phase: N/A
Study type: Observational [Patient Registry]

The efficacy and safety of a novel oral Xa inhibitor for stroke and systemic embolism, namely rivaroxaban, in non-valvular atrial fibrillation patients are evaluated in Japanese clinical practice.

NCT ID: NCT02138695 Recruiting - Atrial Fibrillation Clinical Trials

The Evaluation for Prognostic Factors After Catheter Ablation of Atrial Fibrillation: Cohort Study

Start date: May 2014
Phase:
Study type: Observational

1. Purpose of the study 1) To explore clinical recurrence associated clinical factors including age, sex, clinical, electrophysiological, anatomical, imaging, and serologic characteristics. 2) To develop simulation model to predict clinical recurrence and the efficacy of catheter ablation 2. Scientific evidence of the study 1. In atrial fibrillation patients, the maintenance of normal sinus rhythm showed significant reduction of mortality. 2. drug therapy with anti-arrhythmic drug showed many complications and side effect, thus non-drug therapy such as catheter ablation is developed. 3. catheter ablation has been performed for 10years world-wide, and showed superior treatment outcome compared with drug therapy. 4. clinical outcome after catheter ablation is affected not only by age, sex and underlying disease, but also by electrophysiologic, imaging, serologic and electroanatomical remodeling of the heart. However, there are few studies concerning these multifactorial variables. 3. Study population

NCT ID: NCT02137187 Recruiting - Clinical trials for Permanent Atrial Fibrillation

Atrioventricular Junction Ablation and Biventricular Pacing for Atrial Fibrillation and Heart Failure

APAF-CRT
Start date: October 15, 2014
Phase: Phase 3
Study type: Interventional

There is evidence of superiority of AV junction ablation strategy over pharmacological therapy only for symptoms of atrial fibrillation, but not for heart failure, hospitalization, morbidity and mortality. Hypothesis of trial is that AV junction ablation is superior to pharmacological therapy as regard hospitalization and mortality

NCT ID: NCT02129920 Recruiting - Atrial Fibrillation Clinical Trials

RELAXED: Recurrent Embolism Lessened by Rivaroxaban for Acute Ischemic Stroke

RELAXED
Start date: February 2014
Phase: N/A
Study type: Observational [Patient Registry]

Early recurrence of cardioembolic stroke in patients with atrial fibrillation is common, reaching approximately 6% within 30 days after initial stroke. Therefore, it is preferable to provide early anticoagulation for cardioembolic stroke. However, early anticoagulation may increase the risk of hemorrhagic transformation of cerebral infarcts. It is difficult to decide the timing of initiation for anticoagulant therapy in stroke patients with non-valvular atrial fibrillation (NVAF). In 2013 the European Heart Rhythm Association presented the practical guides for oral anticoagulants in NVAF patients, which recommend that the optimal time to start anticoagulant therapy should be determined according to the stroke severity. However, this recommendation is principally an experts' opinion and is not suitable in the clinical practice in Japan. RELAXED, a multicenter observational study is planned to evaluate the efficacy and safety of an oral direct activated coagulation factor Xa inhibitor, rivaroxaban, for acute ischemic stroke patients with NVAF in consideration of the infarct size, timing of initiation for rivaroxaban medication, and other patient characteristics, and thereby to determine the optimal timing of the initiation during acute ischemic stroke. The consecutive acute ischemic stroke / transient ischemic attack (TIA) patients with NVAF who are treated with rivaroxaban will be enrolled. The infarction size at 0-48 hours after stroke onset will be measured by the diffusion weighted image (DWI) MRI. The primary efficacy endpoint is recurrent ischemic stroke within 3 months. The primary safety endpoint is major bleedings within 3 months. The optimal timing to initiate rivaroxaban during acute ischemic stroke is determined by analysis of co-relation between primary endpoints and the infarct size / time to initiate rivaroxaban.

NCT ID: NCT02110537 Recruiting - Clinical trials for Persistent Atrial Fibrillation

Acupuncture in Persistent Atrial Fibrillation

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

The aim of this trial is to evaluate the effect of acupuncture on prevention of atrial fibrillation (AF) recurrence after electrical cardioversion (EC) for persistent AF patients resistant to the antiarrhythmic drugs (AADs).

NCT ID: NCT02074826 Recruiting - Atrial Fibrillation Clinical Trials

Left Atrial Low vOltage Zone, GenetIC Markers and Outcomes in Patients After Atrial Fibrillation abLation

LOGICAL
Start date: March 2014
Phase: N/A
Study type: Observational [Patient Registry]

This prospective, single-centre cohort study aims to investigate the association between known genetic Atrial Fibrillation (AF) risk variants and the amount of left atrial fibrosis found in patients undergoing clinically indicated AF catheter ablation procedures. Left atrial fibrosis is increasingly recognized as a fundamental part of the pathomorphological substrate creating an electrophysiological environment needed for electrical conduction heterogeneities. Such identification and treatment of left atrial fibrosis has already entered routine clinical use for RF catheter ablation in an attempt to develop an individualized and tailored treatment strategy. Today, it is unclear what impacts the development, the extent and the localization of left atrial fibrosis in different patients. A number of genetic risk variants have been described that confer risk of AF and have been widely replicated. This indicates that genetic variants contribute to the risk of the individual to develop AF throughout his life. However, the mechanisms of how genetic variant impact the development of clinical arrhythmias is not yet well understood. We hypothesize that genetic influences that lead to tissue changes may play a role in the development of the arrhythmia substrate for AF. This is likely to be especially true for those with a relatively brief history of AF and modest clinical disease burden. Therefore, we plan to investigate the association between known genetic AF variants and a detailed disease phenotype obtained from individual left atrial voltage mapping.

NCT ID: NCT02062957 Recruiting - PAT Result Clinical Trials

Endovascular Function in Atrial Fibrillation (AF) Patients

HEAF
Start date: February 2014
Phase: N/A
Study type: Observational

1. recruit 50 patients with atrial fibrillation and 30 controls 2. endovascular function assessment with Peripheral Arterial Tonometry (PAT) 3. follow up the occurence of AF

NCT ID: NCT02051621 Recruiting - Atrial Fibrillation Clinical Trials

Therapy of Atrial Flutter by Afib Ablation

TripleA
Start date: August 2010
Phase: N/A
Study type: Interventional

Ablation of the cavotricuspid isthmus (CTI) in the right atrium is currently the therapy of choice for the treatment of typical atrial flutter (3,4). It is a curative approach and has a high success rate (5). It has been recognized that patients with typical atrial flutter often complain of atrial fibrillation (1,2). Current clinical and experimental studies confirm the close relationship between atrial flutter (AFL) and atrial fibrillation (AF) and raise a question, if both arrhythmias are different forms of a common electrical phenomenon with atrial fibrillation being the underlying clinical problem (6).