Atrial Fibrillation/Sinus Rhythm Before and After Cardioversion

Completed

• Conditions: Atrial Fibrillation

• Registration Number: NCT01779674
• Lead Sponsor: RWTH Aachen University

Brief Summary

This study´s aim is to collect scientific data about patients with atrial inflammation by two principles of sensors measuring congestive heart failure.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-08
• Primary Completion: 2012-04
• Study Completion: 2012-04
• Study First Submitted: 2013-01-28
• Study First Submitted QC: 2013-01-28
• Study First Posted: 2013-01-30
• Status Verified: 2014-01
• Last Update Submitted: 2014-01-07
• Last Update Posted: 2014-01-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• patients with atrial fibrillation and planned cardioversion
• male and female patients aged at least 18 years
• patients being able to understand and to follow the study staff´s instructions
• signed informed consent

Exclusion Criteria

• persons being hosted in an institution by administrative order or court injunction
• pregnancy or breast feeding
• persons not being able to consent
• persons with implanted electronic devices
• material incompatiblity
• acute or chronic inflammation of the external or middle ear canal
• abnormal anatomic ear canal (congenital or pathological)
• persons in a dependent relationship to the investigator or employment contract

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
scientific data	1 hour

Trial Locations

Locations (1)

Univeristy Hospital Aachen; 🇩🇪 Aachen, North Rhine Westfalia, Germany