Condition: Atrial Fibrillation · Atrial Flutter · Sponsor: Population Health Research Institute
This is a multicentre prospective cohort study where patients will receive up to 14 days of continuous ECG monitoring by wearing a portable monitoring device, starting within 72 hours after noncardiac surgery.
This description comes directly from the study's public registry record.
Vitheya Thanabalan · +1 905-296-2710 · detectpoaf@phri.ca
Kate Brady · detectpoaf@phri.ca
Always discuss trial participation with your own doctor first.
| Hamilton General Hospital | Hamilton, Ontario, Canada | Recruiting |
| St. Joseph's Healthcare Hamilton | Hamilton, Ontario, Canada | Not Yet Recruiting |
| Juravinski Hospital | Hamilton, Ontario, Canada | Recruiting |
| London Health Sciences Centre - University Hospital | London, Ontario, Canada | Not Yet Recruiting |
| Niagara Health System - St. Catharine's Site | St. Catharines, Ontario, Canada | Not Yet Recruiting |
| Hôpital Fleurimont du Centre hospitalier universitaire de Sherbrooke | Sherbrooke, Quebec, Canada | Not Yet Recruiting |
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06519747