About this trial
This study aims to assess the percent and risk factors of postoperative atrial fibrillation in patients undergoing cardiac surgery in Assiut university heart hospital
Eligibility criteria
This trial accepts healthy volunteersQualifiers
≥18 years scheduled for first-time planned cardiac surgery ( CABG and Valve replacement)
Patients who are in sinus rhythm and not taking any antiarrhythmic medication, other than beta-adrenergic blocking agents, at the time of surgery.
Willingness to participate and provision of informed consent
Disqualifiers
Prior history of cardiac surgery.
Pediatric population less than 18 years.
Patients with history of hyperthyroidism
Patients with electrolyte disturbance
Trial population
1. ≥18 years scheduled for first-time planned cardiac surgery ( CABG and Valve replacement) 2. Patients who are in sinus rhythm and not taking any antiarrhythmic medication, other than beta-adrenergic blocking agents, at the time of surgery. 3. Willingness to participate and provision of informed consent
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Post operative atrial fibrillation
Prevelance of post operative atrial fibrillation in patients undergoing cardiac surgery ( past CABG and valve replacement )
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: