Atrial Fibrillation Detection using Photoplethysmography at the Wrist

Completed

• Conditions: Atrial Fibrillation; Supraventricular Tachycardia; 10007521

• Registration Number: NL-OMON42452
• Lead Sponsor: Catharina-ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

In order to be eligible to participate in this study, a subject must have been diagnosed with Atrial Fibrillation and either be scheduled to have an elective electrical cardioversion (Phase 1), or be scheduled for a Holter recording (Phase 2). For Phase 2B patients are eligible when they are waiting for an ablation procedure.

Exclusion Criteria

A potential subject will be excluded from participation in this study if he/she is not able to provide informed consent.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>The main study parameters are simultaneous ECG, PPG, and accelerometer<br /><br>recordings that can be used to develop AF detection algorithms.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable.</p><br>