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Clinical Trial Summary

The objective of the study is to evaluate the clinical consequences following the detection of postoperative atrial fibrillation or flutter (POAF) using a remote heart rhythm monitoring strategy with a photoplethysmography based smartphone technology in the early postoperative period after discharge.


Clinical Trial Description

A predefined subgroup analysis of the outcomes described below will be performed in the following subgroups: - Subjects not on anticoagulation drug therapy (for a planned duration of >45 days) at discharge. - Subjects with no history of AF prior to surgery and no POAF lasting >24h in hospital. - Subjects with a CHADSVASC score ≥ 4 or a CHADSVASC score ≥ 2 with at least one additional risk factor associated with the risk of developing POAF. additional risk factors include: - chronic obstructive pulmonary disease - sleep apnea - impaired renal function - left atrial enlargement - elevated body mass index - combined CABG with valve repair or replacement ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05509517
Study type Interventional
Source Universitaire Ziekenhuizen KU Leuven
Contact
Status Completed
Phase N/A
Start date November 2, 2021
Completion date September 4, 2023

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