The Effectiveness of Patch-Based Screening for Pre-Symptomatic Atrial Fibrillation to Improve Patient Outcome

NANot yet recruitingINTERVENTIONAL
Enrollment

24,060

Participants

Timeline

Start Date

June 1, 2026

Primary Completion Date

October 1, 2032

Study Completion Date

October 3, 2033

Conditions
Atrial Fibrillation
Interventions
DEVICE

Zio XT® Patch

For participants randomized to be systematically screened, ambulatory ECG monitoring of up to 14 days will be performed using the Zio XT® Patch (iRhythm Inc, San Francisco, CA). The Zio XT® patch is a small, cutaneous ambulatory ECG recording device that provides cardiac rhythm monitoring for up to 14 consecutive days (significantly longer than the 48 hours of monitoring provided by a typical Holter Monitor). The device is approved by the Food and Drug Administration and is in routine clinical use, including in the VA system.

Trial Locations (1)

94304-1207

VA Palo Alto Health Care System, Palo Alto, CA, Palo Alto

All Listed Sponsors
lead

VA Office of Research and Development

FED

NCT06953778 - The Effectiveness of Patch-Based Screening for Pre-Symptomatic Atrial Fibrillation to Improve Patient Outcome | Biotech Hunter | Biotech Hunter