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Atrial Fibrillation clinical trials

View clinical trials related to Atrial Fibrillation.

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NCT ID: NCT00674401 Completed - Atrial Fibrillation Clinical Trials

Radiofrequency Ablation of Drivers of Atrial Fibrillation

RADAR-AF
Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the value of ablation of high frequency sources following circumferential pulmonary veins isolation in patients with paroxysmal and persistent atrial fibrillation.

NCT ID: NCT00671905 Completed - Atrial Fibrillation Clinical Trials

Circumferential Versus Ganglionated Plexi Ablation for Atrial Fibrillation (AF)

Start date: May 2008
Phase: N/A
Study type: Interventional

The investigators have recently shown that anatomic ganglionated plexi (GP) ablation is inferior to circumferential pulmonary vein (PV) ablation for the treatment of paroxysmal AF. In this study, however, 26% of patients subjected to GP ablation alone without circumferential lesions were free of AF-recurrence up to one year after the ablation procedure. The investigators hypothesized that a combination of circumferential ablation with high-frequency-stimulation-identified GP ablation is superior to conventional circumferential ablation for the prevention of recurrences of paroxysmal atrial fibrillation (AF). The investigators are, therefore, conducting a randomized study comparing conventional circumferential ablation to a combination of circumferential ablation plus specific right and left atrial GP ablation in patients with drug-refractory paroxysmal AF.

NCT ID: NCT00668759 Completed - Atrial Fibrillation Clinical Trials

A Phase III Superiority Study of Vernakalant vs Amiodarone in Subjects With Recent Onset Atrial Fibrillation

AVRO
Start date: April 2008
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to demonstrate the superiority of vernakalant injection over amiodarone injection in the conversion of atrial fibrillation (AF) to sinus rhythm (SR) within 90 minutes of the start of drug administration. The secondary objective is to compare the safety of vernakalant to amiodarone.

NCT ID: NCT00664807 Completed - Atrial Fibrillation Clinical Trials

Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study)

GAME
Start date: April 2008
Phase: Phase 4
Study type: Observational

To generate a list of potential genetic markers that correlate with an increased risk of life-threatening arrhythmias. To evaluate ECG-based risk markers such as heart rate variability and T-wave Alternans for their association with arrhythmic events.

NCT ID: NCT00662701 Completed - Atrial Fibrillation Clinical Trials

Ablation or Surgery for Atrial Fibrillation (AF) Treatment

FAST
Start date: May 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to compare 2 invasive strategies for Atrial Fibrillation treatment, Endocardial catheter ablation isolation of the Pulmonary veins versus minimally invasive thoracoscopic surgical epicardial isolation. Both strategies are in use for several years now, and have been reported as a successful strategy with success rates of 60-90%. However, it is not known which technique is preferable in a given patient population in terms of efficacy to cure AF, safety, or patient discomfort. Therefore, in the present trial a randomized study is proposed to provide more insight into the relative merits of both techniques

NCT ID: NCT00654290 Completed - Atrial Fibrillation Clinical Trials

Effect of Prophylaxy of Amiodarone and Propranolol and Amiodarone With Propranolol in Prevention of Atrial Fibrillation Post Coronary Artery Bypass Graft

Start date: March 2007
Phase: N/A
Study type: Interventional

Atrial fibrillation is the most common arrhythmia post coronary bypass surgery, currently B-blockers are the class I indication to prevent AF post CABG. We decide to evaluate use of propranolol and amiodarone separately and together to find a better prophylaxis for AF peri-CABG

NCT ID: NCT00652522 Completed - Heart Failure Clinical Trials

Atrial Fibrillation Management in Congestive Heart Failure With Ablation

AMICA
Start date: January 2008
Phase: N/A
Study type: Interventional

It is the purpose of the study to show the benefit of the endocardial catheter ablation by pulmonary vein isolation in patients with persistent or longstanding persistent atrial fibrillation, low LVEF and requiring ICD or CRT-D therapy compared to the best medical treatment with antiarrhythmic drugs.

NCT ID: NCT00650728 Completed - Atrial Fibrillation Clinical Trials

Esophagus Imaging for Radiofrequency Ablation of Atrial Fibrillation

Start date: March 2008
Phase: N/A
Study type: Interventional

As the left atrium is in close vicinity to the esophagus, radiofrequency ablation in the left atrium may damage the esophagus and create esophageal perforations and esophageal left atrial fistula. The aim of the present study is to compare different methods for visualization of the esophagus to prevent this complication.

NCT ID: NCT00646997 Completed - Atrial Fibrillation Clinical Trials

Impact of Left Atrial Function on Postoperative Atrial Fibrillation

Start date: March 2008
Phase: N/A
Study type: Observational

We aimed to demonstrate the impact of left atrial functions which were evaluated by three different echocardiographic modalities , on postoperative atrial fibrillation.

NCT ID: NCT00645853 Completed - Clinical trials for Persistent or Permanent Nonvalvular Atrial Fibrillation

Long-term Safety in Atrial Fibrillation Patients

Start date: October 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to provide safety and tolerability data for AZD0837 during long-term treatment (5 years) in patients with non-valvular atrial fibrillation (AF) and one or more additional risk factors for stroke and systemic embolic events (moderate to high risk patients).