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Atrial Fibrillation clinical trials

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NCT ID: NCT03508258 Withdrawn - Clinical trials for Non-valvular Atrial Fibrillation

Study to Describe Risk of Bleeding in Patients Depending on the Different Anticoagulant Therapy They Are on for Atrial Fibrillation (AF)

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

Study of patients with nonvalvular atrial fibrillation (NVAF) who are newly prescribed NOACs (Novel Oral Anticoagulants) in routine clinical practice in England

NCT ID: NCT03489096 Withdrawn - Atrial Fibrillation Clinical Trials

Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation

CANARI-AF
Start date: October 2019
Phase: N/A
Study type: Interventional

Pulmonary vein isolation (PVI) using cryoballoon ablation is a well-established procedure for the treatment of atrial fibrillation (AF). However, the use of cryoballoon ablation in recent clinical trials have been limited to PVI. As such, patients with paroxysmal AF have been the main recipients of this procedure. In patients with persistent AF, or patients with paroxysmal AF and significant AF substrate other than the pulmonary veins, the utility of cryoballoon ablation is less straightforward. In such patients, the choices are to either use cryoballoon ablation in a PVI-only approach or alternatively, use cryoballoon ablation for PVI followed by the use of radiofrequency ablation for additional ablation and/or substrate modification. Substrate modification by targeting left atrial fibrosis detected on delayed enhancement magnetic resonance imaging (DE-MRI) is an increasingly popular approach with growing data showing its utility to decrease the risk of recurrence. The ability to use cryoballoon ablation for fibrosis based ablation in addition to PVI will therefore provide a significant advantage. This study will evaluate feasibility and the outcome of targeted ablation of left atrial fibrosis detected on DE-MRI in addition to pulmonary vein isolation using the Arctic Front Advance Cryoballoon Catheter.

NCT ID: NCT03446222 Withdrawn - Clinical trials for Persistent Atrial Fibrillation

Epicardial Mini-Maze Versus Catheter Ablation for the Management of Persistent Atrial Fibrillation

EMMCAF
Start date: June 2016
Phase: N/A
Study type: Interventional

This study will assess the efficacy of catheter ablation versus the Wolf Mini-Maze surgical ablation for rhythm control in patients with persistent afib.

NCT ID: NCT03441022 Withdrawn - Atrial Fibrillation Clinical Trials

Continuous Data Collection and Analysis for Stroke Prevention Using a Wearable Sensor

Start date: July 15, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a wristband that detects your pulse can detect your heart rate and rhythm similar to electrocardiograms (ECG).

NCT ID: NCT03401931 Withdrawn - Clinical trials for Fibrillation, Atrial

Artificial Intelligence Use for the Detection of Atrial Fibrillation Drivers

AI Fib
Start date: January 9, 2018
Phase:
Study type: Observational [Patient Registry]

pilot clinical study, multicenter, prospective, open, nonrandomized

NCT ID: NCT03398434 Withdrawn - Atrial Fibrillation Clinical Trials

Efficacy and Safety of MAA868 in Patients With Atrial Fibrillation

Start date: October 16, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the pharmacokinetics, pharmacodynamics, safety and tolerability of MAA868 compared to apixaban in patients with atrial fibrillation.

NCT ID: NCT03339193 Withdrawn - Stroke Clinical Trials

Procedure RElated Outcomes With the Watchman FLX Left Atrial Appendage Closure Device

REFLX
Start date: January 2016
Phase: N/A
Study type: Observational [Patient Registry]

This study is a single-centre prospective post-market approval of the early experience with the Watchman FLX device for left atrial appendage closure in patients with atrial fibrillation at high risk of thromboembolic stroke and with contraindications to long-term oral antocoagulation therapy.

NCT ID: NCT03269383 Withdrawn - Atrial Fibrillation Clinical Trials

Study to Evaluate the Effectiveness of SGB in Preventing Post-op Atrial Fibrillation

Start date: December 2019
Phase: Phase 4
Study type: Interventional

Atrial fibrillation requires both an initiation trigger and favorable environment for maintenance and the sympathetic and parasympathetic nervous systems play important roles in this regard. Unfortunately, the precise mechanisms of post operative atrial fibrillation (POAF) are still being investigated. This postoperative complication has persisted in spite of efforts to mitigate it pharmacologically with beta blockers and amiodarone, an experience shared by most other cardiac surgery centers. The stellate ganglion is formed by the fusion of the inferior cervical sympathetic ganglion and first thoracic sympathetic ganglion. By modulating the sympathetic component of the autonomic nervous system, stellate ganglion stimulation has been shown to facilitate induction of atrial fibrillation while ablation may reduce or prevent episodes. Human studies have further supported this model. Preliminary studies of perioperative stellate ganglion block (SGB) in cardiac surgery suggest that this technique may reduce or prevent episodes of POAF requiring treatment. The investigator's hypothesis is that SGB reduces the incidence of POAF in cardiac surgery populations.

NCT ID: NCT03242720 Withdrawn - Atrial Fibrillation Clinical Trials

Effects of PAP on Afib Recurrence Risk After Catheter Ablation in OSA Patients

OSA-AFIB
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

With this pilot study, we are hoping to test the feasibility of a larger study in the future and to learn whether positive airway pressure therapy reduces the recurrence risk of atrial fibrillation after successful catheter ablation procedure among patients with atrial fibrillation and obstructive sleep apnea. The results from this study will help us refine the design for a future larger study, and will ultimately improve care of patients with obstructive sleep apnea and atrial fibrillation.

NCT ID: NCT03162120 Withdrawn - Atrial Fibrillation Clinical Trials

Comparison of Effectiveness of Ranolazine Plus Metoprolol Combination vs. FlecainidE pluS Metoprolol Combination in ATrial Fibrillation Recurrences FOllowing PhaRmacological or Electrical CardioverSion of AtRial Fibrillation

PRESERVE-SR
Start date: September 1, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

Atrial fibrillation (AF) is the most common arrhythmia in clinical practice with a prevalence reaching 5% in patients older than 65 years and an incidence that increases progressively with age.1 According to the most recent guidelines, class Ic anti-arrhythmic drugs are considered the first line treatment in patients without significant structural heart disease. Flecainide is effective in preventing AF recurrences in 31-61% of cases according to different studies.2-5 A recent study showed that the combination of Flecainide and Metoprolol improves effective rhythm control in patients with persistent symptomatic AF compared to Flecainide or Metoprolol alone.6 In contrast, the combination of Flecainide and Metoprolol conferred no significant benefit over Flecainide alone in patients with paroxysmal AF. This suggests different underlying mechanisms for paroxysmal and persistent AF. Pulmonary veins are likely the main focus triggering paroxysmal AF while in persistent AF the role of pulmonary veins is less important.