Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00863382

Comparison of External Event Recorders for Atrial Fibrillation Monitoring

Comparison of External Event Recorders With Implantable Monitor for Post Atrial Fibrillation Monitoring: Assessment of Cost and Efficacy

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Dhanunjaya Lakkireddy, MD, FACC · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Ablation of atrial fibrillation is a well established treatment method to restore normal sinus rhythm and eliminate the need for continued antiarrhythmic therapy and anticoagulation. Absence of symptomatic and asymptomatic atrial fibrillation should be considered necessary for discontinuation of anticoagulation therapy. Presently, recurrence of atrial fibrillation is usually determined with the use of a non looping event monitor which is typically used by the subject at the time of symptomatic arrhythmia. This method does not detect asymptomatic atrial fibrillation. Random asymptomatic recording can be added, but the chance for detecting recurrence of arrhythmia is not great. Too frequently, the success rates of AF ablation procedures are inflated by insufficient follow up and patient's limited compliance in reporting and recording episodes of recurrent arrhythmias. Often times, it is very inconvenient for patients to wear external event recorders. Allergies to the sticky pads that are needed for most of the external monitoring devices continues to be a problem. Implantable loop recorders have the advantage of detecting symptomatic and asymptomatic atrial fibrillation continuously. They also offer the convenience of monitoring for up to 18 to 24 months without significant patient discomfort. However, implantation and explantation of these devices involves a limited surgical procedure as well as considerable experience. In this study we attempt to assess the differences in these two types of monitoring systems in assessing the long term efficacy of AF ablation.

Conditions

Interventions

TypeNameDescription
DEVICEStandard Event MonitorStandard Event Monitor
DEVICESleuth MonitorImplantable Sleuth Recorder

Timeline

Start date
2009-01-01
Primary completion
2011-01-01
Completion
2012-01-01
First posted
2009-03-18
Last updated
2012-05-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00863382. Inclusion in this directory is not an endorsement.