The Box 2.0: using smart technology for early diagnosis of complications after cardiovascular surgery

Recruiting

• Conditions: afib; Atrial fibrillation; 10007521; 10007593

• Registration Number: NL-OMON48739
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Trial is onging in other countries

Detailed Description

Not available

Study Timeline

• Study Completion: 2021-03-15
• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 365

Inclusion Criteria

Patient undergoes cardiovascular surgery
Patient is able to communicate in Dutch or English
Patient has been referred by a cardiologist from the Leiden University Medical
Center, Cardiological Center Voorschoten, Alrijne Hospital or Haaglanden
Medical Center

Exclusion Criteria

Patient is under the age of 18 years
Patient is pregnant
Patient is considered an incapacitated adult
Patient is unwilling to sign the informed consent form
Patient undergoes emergency thoracic surgery (INTERMACS 1 or 2)
Patient has active endocarditis at the time of operation
Patient is on mechanical circulatory support before operation
Patient has a ventricular septal rupture
Patient undergoes extracorporeal membrane oxygenation or ventricular assist
device insertion

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint of the study will be the diagnosis of atrial fibrillation.</p><br>