The Occurrence of Atrial Fibrillation After Totally Endoscopic Cardiac Surgery (AFMICS-II)

Jessa Hospital

Status: Terminated

Conditions: Atrial Fibrillation

Treatments: Device: FibriCheck

Study type: Interventional

Funder types: Other

Identifiers

NCT05633797

f/2022/127

Details and patient eligibility

About

The aim of this study is to investigate the occurrence of new-onset postoperative atrial fibrillation after totally endoscopic cardiac surgery.

Enrollment: 152 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• >18 years old
• Patients undergoing elective endoscopic cardiac surgery (totally endoscopic coronary artery bypass grafting or endoscopic valve replacement)

Exclusion criteria

• Preoperative atrial fibrillation
• Patients that do not understand Dutch or French or English
• Patients that do not have a smartphone
• Concomitant or redo surgeries

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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152 participants in 1 patient group

Totally endoscopic cardiac surgery

Experimental group

Description:

Patients will be monitored using the FibriCheck application to detect atrial fibrillation until 30 days postoperative.

Treatment:

Device: FibriCheck