NCT02898545

Recurrent Atrial Fibrillation

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 1 (actual)
• Sponsor: University of Cincinnati · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This study will evaluate the recurrence rates of atrial fibrillation that develops in the hospital following non cardiac procedures or surgeries or acute medical illnesses.

Detailed description

Eligible individuals with no previous history of atrial fibrillation or flutter who develop a limited episode of atrial fibrillation during a hospital stay for an acute medical illness or non-cardiothoracic surgery or procedure. Patients will be monitored for a period of 1 month using Medtronic SEEQ monitors for recurrence. Subjects will self assign to wear the SEEQ monitor or standard of care. Individuals with implanted cardiac devices capable of detecting atrial fibrillation will also be included.

Conditions

• Atrial Fibrillation

Interventions

Type	Name	Description
DEVICE	SEEQ monitor	An external cardiac rhythm monitor

Timeline

• Start date: 2016-09-01
• Primary completion: 2017-07-20
• Completion: 2017-07-20
• First posted: 2016-09-13
• Last updated: 2017-08-01

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study