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Clinical Trial Summary

This is a cross-sectional study including patients with permanent atrial fibrillation. Assessment will include:

- clinic blood pressure measurements (mercury sphygmomanometer and automated oscillometric device)

- 24-hour ambulatory blood pressure monitoring

- determination of various serum markers and cardiac ultrasound.

- evaluation of a 24h ambulatory blood pressure monitoring device (Microlife WatchBPO3) in terms of its diagnostic value for the detection of atrial fibrillation compared with the reference 24h Holter ECG


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01088269
Study type Observational
Source University of Athens
Contact George S Stergiou, MD
Phone +302107763117
Email gstergi@med.uoa.gr
Status Recruiting
Phase N/A
Start date March 2010
Completion date December 2017

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