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Paroxysmal Atrial Fibrillation clinical trials

View clinical trials related to Paroxysmal Atrial Fibrillation.

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NCT ID: NCT02002988 Recruiting - Clinical trials for Paroxysmal Atrial Fibrillation

Botulinum Toxin Injection Prevent Paroxysmal Atrial Fibrillation

Start date: June 2013
Phase: Phase 1
Study type: Interventional

The aim of this prospective non-randomized study was to assess the efficacy and safety of endomyocardial botulinum toxin injection in projections of main ganglionated plexuses of left atrium for preventing drug-resistant paroxysmal atrial fibrillation.

NCT ID: NCT02002923 Recruiting - Clinical trials for Paroxysmal Atrial Fibrillation

Pulmonary Vein Isolation Versus Botulinum Toxin Injection Plus Pulmonary Vein Isolation in Patients With Atrial Fibrillation

Start date: June 2013
Phase: Phase 2
Study type: Interventional

The investigators have conducted a prospective, double-blind, randomized study to assess the comparative safety and efficacy of two different treatment strategies, PVI only versus PVI plus BT injection, in patients with persistent and paroxysmal AF. Results were assessed after follow-up of at least 1 years with the use of an implanted monitoring device (IMD).

NCT ID: NCT01997736 Completed - Clinical trials for Paroxysmal Atrial Fibrillation

Pilot Study Evaluating the Toray Satake Balloon Thermal Ablation System for Treatment of Paroxysmal Atrial Fibrillation

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

The purpose of this study is to collect preliminary safety and effectiveness data evaluating the Toray Satake Balloon Thermal Ablation System (TSB)to treat subjects with symptomatic paroxysmal atrial fibrillation that is resistant to antiarrhythmic drug therapy.

NCT ID: NCT01959425 Terminated - Clinical trials for Paroxysmal Atrial Fibrillation

Oral Anticoagulation Therapy Pilot Study

OAT
Start date: April 17, 2013
Phase: Phase 4
Study type: Interventional

The objective of this study is to determine the safety of discontinuing oral anticoagulation therapy in high risk patients who have had a successful cardiac ablation and remain AF recurrence free for 3 months post ablation.

NCT ID: NCT01925885 Terminated - Clinical trials for Paroxysmal Atrial Fibrillation

Focal Impulse and Rotor Modulation Ablation Trial for Treatment of Paroxysmal Atrial Fibrillation (FIRMAT-PAF)

FIRMAT-PAF
Start date: September 2013
Phase: N/A
Study type: Interventional

- Hypothesis: Focal Impulse and Rotor Modulation (FIRM) will substantially reduce or eliminate clinical atrial fibrillation in subjects with accepted indications for catheter ablation of paroxysmal AF, compared to standard pulmonary vein isolation. - Summary: This is a prospective randomized study to assess the safety and effectiveness of FIRM procedures only, versus standard Pulmonary Vein Isolation (PVI) procedures for the treatment of symptomatic paroxysmal atrial fibrillation.

NCT ID: NCT01920295 Completed - Clinical trials for Paroxysmal Atrial Fibrillation

Safety and Efficacy of Cryoballoon Ablation of Atrial Fibrillation as First-line Therapy

C-frost
Start date: January 2011
Phase: N/A
Study type: Interventional

Cryoballoon ablation of paroxysmal atrial fibrillation can be used as first-line therapy compared to second choice after failed medical therapy

NCT ID: NCT01917981 Withdrawn - Stroke Clinical Trials

Testing the Accuracy of a Personal Heart Rhythm Monitor to Detect Prolonged Paroxysmal Atrial Fibrillation

Start date: September 2013
Phase: Phase 3
Study type: Interventional

This study aims to determine the sensitivity and specificity of a Personal Heart Rhythm Monitor in the detection of prolonged paroxysmal atrial fibrillation (defined as lasting more than 12 hours) against pre-existing implantable devices, seen to be the 'gold-standard' for arrhythmia detection.

NCT ID: NCT01913522 Completed - Clinical trials for Paroxysmal Atrial Fibrillation

Cryoballoon vs. Irrigated Radiofrequency Catheter Ablation: Double Short vs. Standard Exposure Duration

CIRCA-DOSE
Start date: September 2014
Phase: N/A
Study type: Interventional

Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia and is associated with reductions in quality of life, functional status, cardiac performance, and overall survival.1 Catheter ablation, which is centered on electrical isolation of triggering foci within the pulmonary veins (PVI) through circumferential lesions around PV ostia, has been shown to result in sustained improvements in quality of life, decreased hospitalizations and, potentially, improved survival.2-4 PVI can be accomplished by percutaneous catheter-based thermo-coagulation (burning) with radiofrequency (RF) energy delivery or alternatively by thermo-cooling (freezing) with a cryoballoon catheter.5 Cryothermal ablation with a cryoballoon catheter offers an efficacious means to achieve PVI that is safer than the established technique. Although cryoballoon ablation has been used in clinical practice for sometime, the optimal duration of cryoballoon ablation has not been determined. Moreover, the biophysics of cryo-lesion formation suggests that repeated short freezes ("freeze-thaw-freeze" cycles) may be more efficacious in achieving deep homogenous lesion when compared to prolonged freezing durations. This grant proposal is to verify if repeated short freezing cycles are more efficacious (i.e., fewer recurrence of AF), and safer, than the established standard of long, single freeze cycles.

NCT ID: NCT01912911 Completed - Clinical trials for Paroxysmal Atrial Fibrillation

Evaluating the Efficacy and Feasibility of a Novel Wireless ECG Recording System in Monitoring Patients After Atrial Fibrillation Ablation Procedure

iTransmit
Start date: June 2013
Phase: N/A
Study type: Observational

The investigators goal in this study is to examine the feasibility and efficacy of AliveCor iphone case monitoring device in monitoring patients after AF ablation by comparing transmissions using Alive Cor with transmissions from a traditional transtelephonic monitor (TTM). A secondary goal is to assess the ease of use of AliveCor device compared to traditional TTM system from the patient's perspective

NCT ID: NCT01907828 Completed - Hypertension Clinical Trials

A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and Cardiac Ablation on AF Recurrence

RDN+AF
Start date: April 15, 2014
Phase: N/A
Study type: Interventional

The purpose of this post market clinical investigation is to complete preliminary evaluation on whether or not concomitant renal denervation with the EnligHTN™ Renal Denervation System and cardiac ablation will result in improved outcomes as compared to ablation alone in patients with uncontrolled hypertension being treated for Atrial Fibrillation