Interest of a Hybrid Connected Watch for Cardiac Rhythm Monitoring in Post-operative Cardiac Surgery
Recruiting · NCT05664308 · Observational (researchers observe without assigning treatment) · Lead sponsor: Nantes University Hospital
View the official record on ClinicalTrials.gov →Interventions studied
Clinical follow-up (ECG)Ongoing monitoring
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.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Major with an indication for conventional cardiac surgery with de novo postoperative AF onset.
- Agreeing to participate in the study and having signed an informed consent.
- Agreeing to undergo 12 months of postoperative monitoring.
Exclusion criteria
- Patient with pre-operative AF
- Patient who does not have a smartphone compatible with the connected watch.
- Patient unable to perform an ECG measurement independently.
- Patient with a physical constraint to the measurement (arteriovenous fistula...)
- Minors
- Pregnant or breast-feeding women
- Adults under guardianship, under curatorship
- Patients whose life expectancy is less than 1 year
- Patients participating in another therapeutic trial likely to impact the evaluation criteria of the MONHYCARD study
- Contraindication to long-term anticoagulants
- Patients implanted with a mechanical valve prosthesis pre-operatively or after surgery
Where it is running
1 location listed.
- CHU Nantes - Nantes, Loire Atlantique, France