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Clinical Trial

SmartWatch-driven AF Detection in Stroke Patients

NCT: NCT06832579 · ACTIVE_NOT_RECRUITING

NCT IDNCT06832579
StatusACTIVE_NOT_RECRUITING
Start Date2025-05-15
Completion2026-07

Brief Summary

Unrecognized atrial fibrillation (AF) is a common cause of ischemic stroke. Implantable event monitors (ICM) are the gold standard for continuous heart rhythm monitoring but they have been implemented in very few patients after stroke due to high invasiveness and high costs. In this trial, patients with implanted ICMs (Medtronic Reveal LINQ Insertable Cardiac Monitor) will be randomized to use one of two wearables (1:1 Apple Watch or PulseOn) for continuous monitoring. The aim is to compare the probability of detecting an episode of AF with a wearable versus the gold standard ICM. Both groups will use the wearable for 12 weeks. If the wearables detect an arrhythmic pulse curve, this is communicated by vibration. By laying the other hand on the device, a 1-channel ECG is performed. ECG data will be transferred regularly to the CoreLab (Universityhospital Leipzig) for analysis. After 12 weeks, the patients will visit the site and answer questions regarding the usability, compliance and satisfaction with the wearables.

Frequently Asked Questions

What is SmartWatch-driven AF Detection in Stroke Patients?

SmartWatch-driven AF Detection in Stroke Patients is a clinical trial registered under NCT06832579. Current status: ACTIVE_NOT_RECRUITING.

What is the status of NCT06832579?

The current status of NCT06832579 (SmartWatch-driven AF Detection in Stroke Patients) is: ACTIVE_NOT_RECRUITING.

When did SmartWatch-driven AF Detection in Stroke Patients start?

SmartWatch-driven AF Detection in Stroke Patients started on 2025-05-15.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.