REmote Cardiac MOnitoring of At-risk SYNCope Patients After Emergency Department Discharge -RCT
Recruiting
N/A
Interventional Study
Syncope
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 580 (estimated)
- Sponsor
- Ottawa Hospital Research Institute · Other
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About This Trial
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 wit…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adult patients (aged ≥ 18 years old) who present with syncope to any of the study EDs (within 24 hours), are classified as medium (3-5,) or high-risk (≥6) as per the CSRS and are being discharged from the ED either by the ED team or the consulting team if consulted to another …
Contacts