Clinical Trials Logo

Atrial Flutter clinical trials

View clinical trials related to Atrial Flutter.

Filter by:

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: 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: NCT00243802 Terminated - Atrial Fibrillation Clinical Trials

Markers of Oxidative Stress Present in Left Atrial Appendage Tissue in Patients With Atrial Fibrillation

Start date: May 2005
Phase: Phase 2
Study type: Observational

The purpose of the study is to look at the differences between people who have irregular heart beats coming from the upper chamber of the heart (atrial fibrillation) compared to those who do not have these irregular beats.

NCT ID: NCT00213408 Terminated - Atrial Flutter Clinical Trials

Catheter Ablation as the First Line Therapy for Typical Atrial Flutter

Start date: June 2001
Phase: Phase 4
Study type: Interventional

Catheter ablation of typical atrial flutter is a well established technique with a high acute success rate and very low complication and recurrence rates. It has also been shown that ablation of recurrent symptomatic typical atrial flutter led to a clear improvement in quality of life. We sought to evaluate the cost/effectiveness of catheter ablation as the first line therapy in patient suffering from their first symptomatic typical atrial flutter episode. This study is a multicenter trial in which patients with a first symptomatic episode of typical atrial flutter are randomized to undergo ablation or to receive antiarrhythmic drugs after electrical cardioversion. Clinical examination, quality of life questionnaires,12 leads ECG and 24-hour Holter monitoring are performed at 1, 3, 6 and 12 months following randomization.The primary end-point is the absence of recurrence of typical atrial flutter at - and 12 months of follow up. The secondary end points are the cost and the cost/effectiveness ratio of these two approaches.