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Atrial Fibrillation clinical trials

View clinical trials related to Atrial Fibrillation.

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NCT ID: NCT01259284 Terminated - Advanced Cancers Clinical Trials

Fish Oil Versus Statins Versus Placebos in Reducing Atrial Fibrillation in Patients Undergoing Thoracic Surgery for Lung Cancer

Start date: January 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The goal of this clinical research study is to learn if Lipitor (atorvastatin) or fish oil supplements can help to control side effects of the heart that are commonly seen after lung surgery (such as irregular heartbeat). Researchers also want to learn if one of these drugs is more effective than the other at controlling side effects.

NCT ID: NCT01253590 Terminated - Fibrillation Clinical Trials

Cardiac Monitoring of Post-Operative Cancer Patients Experiencing Atrial Fibrillation

Start date: December 2010
Phase: N/A
Study type: Observational

The purpose of this study is to assess whether it is possible and acceptable to monitor patients at a distance who experience a condition called atrial fibrillation after their cancer surgery. Some patients have no other clinical reason for staying in the hospital after cancer surgery except in order to control their heart rhythm. Being able to send these patients home earlier and monitor them at a distance from their home can be good for their quick recovery. Studies have shown greater quality of life and patient satisfaction when patients are monitored at a distance for conditions like atrial fibrillation, however cancer patients have not been studied.

NCT ID: NCT01233635 Terminated - Atrial Fibrillation Clinical Trials

Secondary Prevention of Atrial Fibrillation (Impact of Renin-Angiotensin-Aldosterone System Inhibition)

Start date: November 2005
Phase: Phase 4
Study type: Interventional

In the present application, we propose to refine and extend current insight into AAF mechanism and therapy by examining the importance of pharmacologic RAAS inhibition, ACE genotype, and their interaction in secondary AF prevention. We have 3 specific aims: 1. To confirm that RAAS inhibition therapy reduces the incidence of AF recurrence. 2. To test the hypothesis that the incidence of AF recurrence in the absence of RAAS inhibition therapy is higher among patients with the D allele. 3. To explore the hypothesis that RAAS inhibition therapy is more effective for preventing AF recurrence in patients with the DD genotype than in those with DI or II genotypes.

NCT ID: NCT01198873 Terminated - Atrial Fibrillation Clinical Trials

Effects of Dronedarone on Cardiac Geometry and Function in Patients With Atrial Fibrillation and Left Atrial Enlargement

ODYSSEUS
Start date: September 2010
Phase: Phase 4
Study type: Interventional

Primary Objective: - Evaluate the effect of dronedarone versus placebo (standard therapy) in slowing the progression of adverse left atrial remodeling in patients with atrial fibrillation (AF) following 12 months of treatment. Secondary Objectives: - Evaluate the effects of dronedarone versus placebo on left atrial function; - Evaluate the effects of dronedarone versus placebo on left atrial dimension; - Evaluate the effects of dronedarone versus placebo on left ventricular function (LVEF, E, E', A, E/E') - Evaluate the safety and tolerability of dronedarone.

NCT ID: NCT01175330 Terminated - Atrial Fibrillation Clinical Trials

Omega 3 Fatty Acid Efficiency for Prevention of Atrial Fibrillation After Coronary Artery Bypass Grafting

Start date: August 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate efficacy of Polyunsaturated Fatty Acid for the prevention of Atrial Fibrillation and anti-inflammatory effects in patients after CABG surgery

NCT ID: NCT01151137 Terminated - Atrial Fibrillation Clinical Trials

Permanent Atrial fibriLLAtion Outcome Study Using Dronedarone on Top of Standard Therapy

PALLAS
Start date: July 2010
Phase: Phase 3
Study type: Interventional

Primary Objective: - Demonstrate the efficacy of Dronedarone in preventing major cardiovascular events (stroke, systemic arterial embolism, myocardial infarction or cardiovascular death) or unplanned cardiovascular hospitalization or death from any cause in patients with permanent Atrial Fibrillation [AF] and additional risk factors Secondary Objective: - Demonstrate the efficacy of Dronedarone in preventing cardiovascular death This was an event-driven study where a common study end date [CSED] was to be determined by Steering Committee based on the number of events (stroke, systemic arterial embolism, myocardial infarction or cardiovascular death).

NCT ID: NCT01144858 Terminated - Clinical trials for Persistent Atrial Fibrillation

Clinical Value of Left Atrial Appendage Flow for Prediction of Successful Catheter Ablation for Persistent Atrial Fibrillation

CLAAAF
Start date: January 2009
Phase: N/A
Study type: Observational

The purpose of this study was to determine whether left atrial appendage flow velocity, as determined using trans esophageal echocardiography (TEE), predicts the outcome after catheter ablation of persistent Atrial fibrillation( pAF).

NCT ID: NCT01135017 Terminated - Atrial Fibrillation Clinical Trials

Effects of Dronedarone on Atrial Fibrillation Burden in Subjects With Permanent Pacemakers

HESTIA
Start date: July 2010
Phase: Phase 4
Study type: Interventional

Primary objective was to evaluate the effects of dronedarone on Atrial Fibrillation (AF) burden (i.e. percent time in AF) as measured on electrogram (EGM) in subjects with a permanent pacemaker. Secondary objectives were to evaluate: - the effects of dronedarone on AF pattern characteristics i.e. ventricular rate during AF; - the effects of dronedarone on subject-perceived AF burden and symptom severity as reported by subjects using the Atrial Fibrillation Severity Scale (AFSS); - the incidence of electrical cardioversion (or overdrive pacing) during treatment; - the safety of dronedarone.

NCT ID: NCT01122173 Terminated - Clinical trials for Paroxysmal Atrial Fibrillation

Use of the Hansen Medical System in Patients With Paroxysmal Atrial Fibrillation

Start date: July 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and performance of the Hansen Medical Sensei Robotic System and Artisan Catheter when used to robotically manipulate RF ablation catheters for the treatment of paroxysmal atrial fibrillation (irregular heartbeats originating in the upper chambers of the heart).

NCT ID: NCT01116557 Terminated - Atrial Fibrillation Clinical Trials

Efficacy, Safety and Efficiency Study of CARTO® 3 System Guided THERMOCOOL® Catheter Ablation Versus Fluoroscopy Guided Ablation With the Pulmonary Vein Ablation Catheter® (PVAC®)

CLARITY-AF
Start date: April 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the efficacy, safety and efficiency of CARTO® 3 system guided THERMOCOOL® catheter ablation and fluoroscopy guided Pulmonary Vein Ablation Catheter® (PVAC®) guided ablation for the treatment of paroxysmal atrial fibrillation.