Clin2
NCT06164808Likely a fitRecruiting

Comparing a wearable heart monitor to a standard Holter monitor

Cardiac ArrhythmiaDiagnostic/Monitoring Devices Related to Adverse IncidentsAtrial Fibrillation (AF)

Part of Heart & circulation clinical trials.

This study compares a new wearable heart monitor (HeartWatch) that you wear on your left bicep to the standard Holter monitor. It aims to see if the HeartWatch is as good at recording your heart's rhythm over 24-48 hours, so you might have a more comfortable option for heart monitoring.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
300 people
Ages
22 years and older
Study type
Interventional

Who can take part

  • You are 22 years of age or older
  • Your doctor has recommended a Holter monitor test (a portable device that records your heartbeat)
  • You can wear the study device on your left upper arm (bicep) for the entire study period
  • Your left bicep measures between 22 cm and 45 cm (about 8.7 to 17.7 inches)
  • You do not have a permanent pacemaker or implantable defibrillator
  • You are not allergic to any parts of the Holter monitor or the study device
  • You do not have a medical condition that prevents wearing the device on your left arm (e.g., a blood clot, dialysis fistula, or nerve pain)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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