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NCT06310707

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

Terminated NA Last updated 8 December 2025
What this trial tests

NA trial testing ePatch ® Extended Wear Holter (EWH) in Arrythmia in 55 participants. Terminated before completion.

Timeline
9 November 2023
Primary endpoint
10 July 2025
10 July 2025

Quick facts

Lead sponsorPhilips Clinical & Medical Affairs Global
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment55
Start date9 November 2023
Primary completion10 July 2025
Estimated completion10 July 2025
Sites2 locations across France, Germany

Drugs / interventions tested

Conditions studied

Sponsor

Philips Clinical & Medical Affairs Global — full company profile →

Who can join

18 and older, any sex, with Arrythmia or Syncope. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own 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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Arrythmia

Currently open trials in the same condition.

Other Philips Clinical & Medical Affairs Global trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06310707.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing