Actively Recruiting
Interest of a Hybrid Connected Watch for Cardiac Rhythm Monitoring in Post-operative Cardiac Surgery
Led by Nantes University Hospital · Updated on 2026-01-30
106
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this single-center pilot study is, with the help of a connected watch, to show the absence of recurrence or maintenance of sinus rhythm in patients with a Post Operative Atrial Fibrillation (POAF) and to help treating cardiologists in the care of these patients.
CONDITIONS
Official Title
Interest of a Hybrid Connected Watch for Cardiac Rhythm Monitoring in Post-operative Cardiac Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be an adult with a new onset of postoperative atrial fibrillation after conventional cardiac surgery
- Agree to participate and provide informed consent
- Agree to undergo 12 months of postoperative heart rhythm monitoring
You will not qualify if you...
- Have pre-operative atrial fibrillation
- Do not have a smartphone compatible with the connected watch
- Unable to perform ECG measurements independently
- Have physical conditions preventing measurement (e.g., arteriovenous fistula)
- Be a minor
- Be pregnant or breastfeeding
- Be under legal guardianship or curatorship
- Have a life expectancy less than 1 year
- Participate in another therapeutic trial affecting this study's evaluation
- Have contraindications to long-term anticoagulants
- Have a mechanical heart valve prosthesis implanted before or after surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU Nantes
Nantes, Loire Atlantique, France, 44093
Actively Recruiting
Research Team
C
Charles-Henri DAVID
CONTACT
I
Imen FELLAH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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