NCT05664308Recruiting
Interest of a Hybrid Connected Watch for Cardiac Rhythm Monitoring in Post-operative Cardiac Surgery
Single-center Pilot Study to Evaluate the Interest of a Hybrid Connected Watch for Heart Rate Monitoring in Postoperative Cardiac Surgery
Source: ClinicalTrials.gov · Last updated 29 Sept 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 106 (estimated)
- First submitted
- 14 Dec 2022
- Start date
- 19 Mar 2024
- Primary completion date
- 19 Mar 2028
- Lead sponsor
- Nantes University Hospital
- Diseases
- Atrial fibrillation
- NCT number
- NCT05664308
What you commit to
- Study type: Observational
- Planned participants: 106
- From 19 Mar 2024 to the primary completion date, 19 Mar 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients implanted with a mechanical valve prosthesis pre-operatively or after surgery
Other illness
- Patient with a physical constraint to the measurement (arteriovenous fistula...)
Other
- 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.
- 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
Who the study is looking for
- 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.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU Nantes Coordinator of this site? Confirm its status | Nantes | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.