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Atrial Fibrillation clinical trials

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NCT ID: NCT00583921 Withdrawn - Atrial Fibrillation Clinical Trials

Ventricular Rate Regularization for Improved Quality of Life in Patients With CHF and AF

VRR
Start date: n/a
Phase: N/A
Study type: Observational

Single center investigator initiated sponsored by Guidant Boston Scientific Corp. to evaluate the benefit of ventricular rate regularization (VRR) in patients with congestive heart failure (CHF) and significant atrial fibrillation (AF) burden.

NCT ID: NCT00571779 Withdrawn - Atrial Fibrillation Clinical Trials

AtriCure Minimally Invasive Surgical Ablation for Atrial Fibrillation/RESTORE IIB

RESTORE SR IIB
Start date: n/a
Phase: Phase 2
Study type: Interventional

Feasibility study arm to evaluate the safety of adding the left atrial linear connecting lesions of the Cox-Maze lesion set to the current RESTORE SR II IDE study procedure of performing pulmonary vein isolation, selected left atrial autonomic ganglionated plexi (GP) ablation, and optional left atrial appendage (LAA) excision/exclusion on a beating heart for patients with permanent or persistent Atrial Fibrillation (AF).

NCT ID: NCT00510900 Withdrawn - Atrial Fibrillation Clinical Trials

Effects of Left Atrial Appendage Occlusion

Start date: August 2005
Phase: N/A
Study type: Observational

The proposed work seeks to further understand the effects of LAA occlusion on cardiac structure and function, and in homeostasis. Numerous studies have implicated the left atrial appendage (LAA) as the source of the vast majority of left atrial thrombi in the setting of AF3. The University of Pittsburgh Medical Center will be implanting a Left Atrial Appendage filter system (the WATCHMAN® Left Atrial Appendage Filter System, manufactured by Atritech, Inc.). We aim to follow these patients for six months post implant in order to assess their heart rhythm, function, and to do blood tests to evaluate for neurohormonal changes.

NCT ID: NCT00508248 Withdrawn - Atrial Fibrillation Clinical Trials

Omega 3 Fatty Acids and Atrial Fibrillation

Start date: January 2005
Phase: N/A
Study type: Interventional

Unlike for ventricular arrhythmias, the role of n-3 PUFAs in atrial arrhythmias has not been fully investigated. A recently published epidemiological study reported that in elderly patients, consumption of fish was associated with a lower incidence of atrial fibrillation over the 12 years of follow-up. This observation may be an indirect effect due to the overall beneficial effort of fish consumption on reducing ischaemic heart disease, however this association persisted after adjustment for confounding characteristics. Clinical data regarding the direct impact of n-3 PUFAs on atrial arrhythmias such as atrial fibrillation/flutter (AF) is lacking. However, as both INa and ICa-L are also in atrial myocytes, similar anti-fibrillatory actions by n-3PUFAs would be expected in atrial fibrillation and we would like to investigate this further. The primary aim of this study is to investigate whether dietary supplements of n-3 PUFA concentrates (1g fish oil/day comprising eicosapentaenoic acid, EPA 46% and docosahexaenoic, DHA 38%)) helps maintain sinus rhythm after cardioversion to normal sinus rhythm in patients with persistent atrial fibrillation.

NCT ID: NCT00466973 Withdrawn - Atrial Fibrillation Clinical Trials

Atrial Fibrillation Ablation Device Comparison Study

Start date: April 2007
Phase: Phase 4
Study type: Interventional

Atrial fibrillation is an irregular heart rhythm which requires long term anticoagulation to prevent risk of stroke and long term poor outcomes. At the same time one have heart surgery, a small additional procedure can be done to treat atrial fibrillation. Surgeons have a choice of six different devices that he or she can use to treat your atrial fibrillation. It is not known at this point which device is best at treating you, as each device seems to have the same success rate at curing atrial fibrillation. One of the six devices will be selected randomly by card pulled out at the time of enrollment. It is therefore the purpose of this study to compare the devices to each other and to follow up after surgery to determine if any one device is best. This information will be valuable to surgeons and to patients as the treatment for atrial fibrillation develops in the future.

NCT ID: NCT00369330 Withdrawn - Atrial Fibrillation Clinical Trials

KONVERT-AF - Relevance of Point in Time for Conversion of Acute Atrial Fibrillation

Start date: September 2006
Phase: N/A
Study type: Interventional

To investigate if in acute symptomatic atrial fibrillation (AF) the early (>2 hrs but within 12 hrs of the beginning of the arrhythmia) electrical cardioversion leads to a longer recurrence-free interval than the delayed cardioversion (> 36 hrs but < 48 hrs after the beginning of the arrhythmia) within the first 3 months after cardioversion.

NCT ID: NCT00184249 Withdrawn - Atrial Fibrillation Clinical Trials

A Prospective Multi Centre Trial on Bipolar Radiofrequency Ablation of Atrial Fibrillation

Start date: June 2005
Phase: N/A
Study type: Interventional

The study is a prospective multi-centre study to investigate the effect of a new bipolar ablation strategy of the left atrium in patients with paroxysmal or permanent atrial fibrillation over time.

NCT ID: NCT00115843 Withdrawn - Atrial Fibrillation Clinical Trials

Atrial Fibrillation Rate Control Therapy Guided By Continuous Ambulatory Monitoring

Start date: April 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate that the use of a continuous ambulatory monitoring device will reduce both the time to effective rate control and the health care expenditures associated with standard methods of rate control monitoring in patients presenting with atrial fibrillation with a rapid heart rate.