Atrial Fibrillation/Sinus Rhythm Before and After Cardioversion
NCT ID: NCT01779674
Last Updated: 2014-01-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
25 participants
OBSERVATIONAL
2011-08-31
2012-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Studies of Disorders and Mechanisms Related to Atrial Fibrillation Before and After DC-Conversion.
NCT00429884
Atrial Fibrillation Ablation Registry
NCT03075930
Risk Profile for Patients With Atrial Fibrillation
NCT01510210
Risk Profile for Atrial Fibrillation
NCT01510197
Observational Study of Sinus Rhythm Mapping in Pulmonary Vein Isolation Naive Patients With Atrial Fibrillation
NCT06098664
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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
18 Years
90 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
RWTH Aachen University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Univeristy Hospital Aachen
Aachen, North Rhine Westfalia, Germany
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Zink MD, Bruser C, Winnersbach P, Napp A, Leonhardt S, Marx N, Schauerte P, Mischke K. Heartbeat Cycle Length Detection by a Ballistocardiographic Sensor in Atrial Fibrillation and Sinus Rhythm. Biomed Res Int. 2015;2015:840356. doi: 10.1155/2015/840356. Epub 2015 Jul 1.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
10-079
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.