Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06724718

Diagnosis of Atrial Fibrillation in Postoperative Thoracic Surgery Using a Smartwatch

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
302 (estimated)
Sponsor
Centre Hospitalier Universitaire, Amiens · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
OTHERsmartwatchPatients in the smartwatch group will undergo rhythm monitoring with a smartwatch
OTHERECGDetected POAF episodes will be confirmed via a 12-lead ECG

Timeline

Start date
2025-06-01
Primary completion
2027-07-01
Completion
2027-12-01
First posted
2024-12-09
Last updated
2025-06-12

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06724718. Inclusion in this directory is not an endorsement.