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Study identifier: NCT05066347 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

REmote Cardiac MOnitoring of At-risk SYNCope Patients After Emergency Department Discharge -RCT

Condition: Syncope  ·  Sponsor: Ottawa Hospital Research Institute

PhaseNA
Planned participants580
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Syncope (fainting) is a common reason for emergency department (ED) presentation. Fainting can be caused by heart conditions such as irregular heart rhythm (arrhythmia) that can be life-threatening, structural heart problems, or serious conditions not related to the heart. The standard or usual treatment for the majority of patients at-risk for irregular heart rhythm is getting discharged home with no heart rhythm monitoring. If patients receive any monitoring, only Holter monitoring device that records all heart beats for 24 hours to 72 hours will be used. One-third to half of irregular heart rhythm will be identified only after patients are either discharged from the ED or hospitalized in an inpatient unit. One-third to half of irregular heart rhythm will be identified only after patients are either discharged from the ED or hospitalized in an inpatient unit. The study hypothesize that prolonged live cardiac rhythm monitoring (15 days) of at-risk syncope patients, discharged from the ED, will lead to identification of irregular heart rhythm, which can lead to improved patient safety and lower healthcare costs.

This description comes directly from the study's public registry record.

Talk to the study team

Iris Nguyen, BSc  ·  613-798-5555  ·  pnguyen@ohri.ca

Always discuss trial participation with your own doctor first.

Locations (1)

The Ottawa Hospital - Civic and General CampusesOttawa, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT05066347