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Atrial Fibrillation/Sinus Rhythm Before and After Cardioversion

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01779674
Enrollment
25
Registered
2013-01-30
Start date
2011-08-31
Completion date
2012-04-30
Last updated
2014-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation

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.

Interventions

None listed

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
scientific data1 hour

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026