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Arrhythmia Identification in Syncope Patients: ePatch® Versus 24h Holter

Syncope Clinical Trial

Official title:
A Randomized Controlled Study to Identify Clinically Actionable Arrhythmia Using the ePatch® Extended Wear Holter vs. Standard Wear Holter

Clinical Trial Summary

This study is a Multi-center, prospective, randomized, unblinded, two-arm study to assess if 7-days of cardiac monitoring using the ePatch Holter results in identification of more clinically actionable arrythmia for patients with symptoms of syncope than standard 24 hour Holter monitoring.

Clinical Trial Description

This study is a multi-center, prospective, randomized, unblinded, two-arm study to assess if 7-days of cardiac monitoring using the ePatch Holter results in identification of more clinically actionable arrythmia for patients with symptoms of syncope than standard 24 hour Holter monitoring. Approximately 256 adult subjects with symptoms of syncope will be randomized 1:1 to wear either the Philips ePatch Extended Wear Holter (7 day) or Standard Wear Holter (24 hours). Randomization will be balanced for gender. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06310707
Study type Interventional
Source Philips Clinical & Medical Affairs Global
Contact Purvee Parikh
Phone +1 619-929-6310
Email purvee.parikh@philips.com
Status Recruiting
Phase N/A
Start date November 9, 2023
Completion date August 2025
View Details
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