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Atrial Flutter clinical trials

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NCT ID: NCT00839657 Completed - Stroke Clinical Trials

Clarification of Optimal Anticoagulation Through Genetics

COAG
Start date: September 2009
Phase: Phase 3
Study type: Interventional

Individuals taking warfarin often need frequent dose changes as the international normalized ratio (INR) gets too high or too low which could result in a higher risk of thromboembolism, bleeding and early discontinuation of a highly useful therapy. This study will compare two approaches to warfarin dosing to examine the utility of using genetic information for warfarin dosing.

NCT ID: NCT00750711 Recruiting - Clinical trials for Radiofrequency Ablation

Typical Flutter Ablation:A Comparison of 4 mm Versus 2 mm Irrigated cathéters

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

The purpose of this study is to compare the efficacy of 4 mm irrigated catheters with 2 mm irrigated catheters for ablation of typical flutter.It's a prospective randomised multicenter study.

NCT ID: NCT00736294 Terminated - Atrial Fibrillation Clinical Trials

Prevention of Atrial Fibrillation by Inhibition Conversion Enzyme (ICE) After Radiofrequency Ablation of Atrial Flutter

PREFACE
Start date: July 2008
Phase: Phase 3
Study type: Interventional

Atrial Flutter [AFL] is a relatively frequent arrhythmia, considered as benign, but associated with both invalidating symptoms and thromboembolic risk. The objective of the treatment consists to on the one hand the sinus rhythm [SR] restoration and on the other hand the prevention of the long-term recurrence. In this clinical setting, AFL radiofrequency ablation [RFA] became the first line therapy due to its both high effectiveness and safety. The effectiveness of AFL RFA is attenuated by the subsequent risk of atrial fibrillation [AFib] close to 25% at 1 year. This risk of subsequent AFib is related to the common substrate between both arrhythmias. When AFib occurs, the interest to maintain the SR is still required, even if recent studies did not show a significant difference in term of total mortality between rate or rhythm control strategies [AFFIRM, RACE and PIAF studies]. The studies published underlined the anti-arrhythmic drugs limits in patients with both arrhythmias [AFib and AFL]. After years centered on the mechanisms and the electric treatments of AFib, researchers are nowadays focusing on the study's evaluation of the atrial tissue substrate. Accordingly, the renin-angiotensin system role was investigated in many works. Indeed, angiotensin II plays a role in the modification of atrial pressure and in the fibers stretching ["stretch"], conditions required for the development of AFib. Angiotensin II is also a factor implied in the tissue fibrosis leading to tissue proliferation and collagen alteration. These mechanisms lead to atria cells conduction disorders and refractory periods modification. Moreover, the enzyme of conversion expression and the angiotensin II receptors deterioration were observed in patients with AFib. This brings to the concept of AFib treatment while interfering on tissue remodeling by the way of renin-angiotensin system. Drugs such as the angiotensin converting enzyme inhibition [ACEI] may reduce AFib in patients with heart failure. No randomized study so far has compared the ACEI drugs against placebo among high-risk patients of AFib in post AFL RFA area. On the basis of experimental and clinical study, the investigators seek to evaluate the ACEI use in the prevention of AFib in an AFL post RFA ablation.

NCT ID: NCT00709384 Completed - Atrial Flutter Clinical Trials

Prevention of Atrial Tachycardia After a Right Atriotomy II

Start date: January 2006
Phase: Phase 2
Study type: Interventional

The investigators performed a prophylactic peroperative linear lesions connecting the tricuspid annulus with a right atriotomy and the atriotomy with the inferior caval vein to prevent atrial flutter on 15 consecutive adult patients undergoing surgery for congenital heart disease. Conduction time between electrodes placed on both sides of the lesions is measured on the second postoperative day. Coronary angiography and electrophysiology study using an electroanatomic mapping system to assess conduction across the line are performed three month after the operation.

NCT ID: NCT00691470 Active, not recruiting - Atrial Fibrillation Clinical Trials

Comparison of ATI-5923, a Novel Vitamin K Antagonist, With Warfarin in Patients Requiring Chronic Anticoagulation

EmbraceAC
Start date: May 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this research study is to test an experimental drug ATI-5923 vs Coumadin. The study is intended to demonstrate ATI-5923 is superior to Coumadin for keeping INR values in the desired therapeutic range. Patients who require chronic anticoagulation with one or more of the following conditions are eligible for the study: atrial fibrillation or atrial flutter, prosthetic heart valve, venous thromboembolic disease, or history of myocardial infarction or cardiomyopathy will be enrolled.

NCT ID: NCT00616629 Completed - Atrial Flutter Clinical Trials

Cardiac Electrophysiological Study

Start date: January 2008
Phase: Phase 2
Study type: Interventional

The purpose of the study is to measure the effects of AZD1305 on cardiac electrophysiological properties and intracardiac pressures

NCT ID: NCT00606463 Terminated - Atrial Flutter Clinical Trials

Gen2 Isthmus-Dependent Atrial Flutter Ablation Study

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

Irrigated catheter for ablation of isthmus-dependent atrial flutter

NCT ID: NCT00560872 Completed - Atrial Flutter Clinical Trials

Remote Magnetic Navigation For Cavotricuspid Isthmus Ablation

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

The purpose of this study is to evaluate the influence of remote magnetic catheter navigation on the safety and efficacy of mapping and radiofrequency ablation of the cavotricuspid isthmus in patients with typical atrial flutter.

NCT ID: NCT00559988 Terminated - Stroke Clinical Trials

Combined Use of BIOTRONIK Home Monitoring and Predefined Anticoagulation to Reduce Stroke Risk

IMPACT
Start date: February 2008
Phase: Phase 4
Study type: Interventional

The IMPACT Study will investigate the potential clinical benefit of the combined use of BIOTRONIK Home Monitoring (HM) technology and a predefined anticoagulation plan compared to conventional device evaluation and physician-directed anticoagulation in patients with implanted dual-chamber defibrillators or cardiac resynchronization therapy devices.

NCT ID: NCT00491010 Recruiting - Atrial Flutter Clinical Trials

Maximum Targeted Ablation of Atrial Flutter

Start date: July 2006
Phase: Phase 4
Study type: Interventional

Patients undergoing atrial flutter ablation will be randomized to either the standard ablation approach or voltage targeted approach. Patients will be followed for one year to assess outcome of the ablation technique