Dynamic Data-Driven Management of Atrial Fibrillation Using Implantable Cardiac Monitors: The MONITOR-AF Study

Completed

Conditions studied: Atrial Fibrillation

In brief

Observational, multi-center, retrospective study to evaluate the use of ICM (implantable cardiac monitor) versus traditional, non-ICM (non-implantable cardiac monitor) methods such as ECGs (electrocardiogram), Holter, and mobile cardiac outpatient telemetry (MCOT) units.

Key facts

Study ID

NCT06352060

Run by

Kansas City Heart Rhythm Research Foundation

People needed

598

Starts

2018-01-01

Expected to finish

2021-12-31

Last updated by the study team

2025-04-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients > 18 years of age
• Present for management of AF
• ICM is inserted at the discretion of the treating physician

You may not qualify if…

• Patients < 18 years of age
• Presence of a permanent pacemaker, implantable cardiac defibrillator, or cardiac resynchronization therapy
• Unable to tolerate ICM or traditional monitoring with ECG, Holter, or MCOT monitoring
• Unable to tolerate AAD, OAC, and CA as part of AF standard of care
• ICM inserted for cryptogenic stroke or syncope
• Was not followed > 12 months
• CA performed for AF before ICM implant

Where it is running

• Menorah Medical Center — Overland Park, Kansas, United States
• Kansas City Heart Rhythm Institute - Roe Clinic — Overland Park, Kansas, United States
• Overland Park Regional Medical Center — Overland Park, Kansas, United States
• Centerpoint Medical Center Clinic — Independence, Missouri, United States
• Centerpoint Medical Center — Independence, Missouri, United States
• Research Medical Center Clinic — Kansas City, Missouri, United States
• Research Medical Center — Kansas City, Missouri, United States

Full record on ClinicalTrials.gov

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