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

Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2023
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.
Epistemonikos ID: ebec114622114c3cfc105c0dbf113a9bb851599e
First added on: May 15, 2024