Remote Monitoring of Patients with a Nanostim Leadless Pacemaker Utilizing a Smartphone Enabled ECG

Overview

About this study

The purpose of this study is to observe the remote ECG signals of Nanostim pacemaker patients utilizing the AliveCor device, and compare these ECG signals with ECG recordings collected with the Nanostim device programmer during their clinical follow-up.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Patients with a currently implanted Nanostim leadless pacemaker, being followed at Mayo clinic

Exclusion Criteria: 

  • Patients without the ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Paul Friedman, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Additional contact information

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Phone: 800-664-4542 (toll-free)

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