NCT06724718Recruiting
Diagnosis of Atrial Fibrillation in Postoperative Thoracic Surgery Using a Smartwatch
Source: ClinicalTrials.gov · Last updated 12 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Postoperative atrial fibrillation (POAF) occurs in approximately 20% of patients following thoracic surgery. Early diagnosis is essential to prevent complications such as heart failure, stroke, myocardial infarction, and increased mortality. Smartwatches equipped with single-lead ECG capabilities and algorithms to detect asymptomatic atrial fibrillation (AF) offer a potential solution. This study aims to evaluate the effectiveness of smartwatches in detecting POAF compared to standard care.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 302 (estimated)
- First submitted
- 5 Dec 2024
- Start date
- 1 Jun 2025
- Primary completion date
- Jul 2027
- Lead sponsor
- Centre Hospitalier Universitaire, Amiens
- Diseases
- Atrial fibrillation
- NCT number
- NCT06724718
What you commit to
- Study type: Interventional
- Planned participants: 302
- From 1 Jun 2025 to the primary completion date, Jul 2027
- 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
- Mediastinal, pleural, or chest wall surgery.
- Reoperations or surgeries performed more than 48 hours prior.
Other illness
- History of atrial fibrillation.
Other
- Requirement for telemetry for AV block or tachyarrhythmias (\>140 bpm).
- Dependency on a pacemaker.
- Participation in another interventional clinical trial affecting POAF incidence.
- Pregnant women.
- Patients under guardians or similar legal protection.
Who the study is looking for
- Adults (\>18 years old).
- Patients undergoing major thoracic surgery with one-lung ventilation within the past 48 hours.
- Scheduled pneumonectomy or lobectomy.
- Admission to a conventional surgical unit postoperatively.
- Ability to perform single-lead ECG using a smartwatch.
- Coverage under a social security system.
- Signed informed consent
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 |
|---|---|---|---|
| Centre hospitalier Amiens Coordinator of this site? Confirm its status | Amiens | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.