Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:45 PM
Ignite Modification Date:
2025-12-24 @ 6:45 PM
NCT ID:
NCT04926857
Eligibility Criteria:
Inclusion Criteria
* Patients with a LINQ ICM who have a self-reported history of AF and who have received an ICM for the following device-logged indications, categorized into the following discrete groups:
* AF management: AF management and post-ablation management indications
* Suspected AF: Suspected AF and palpitations indications
* Stroke: Cryptogenic stroke indication
* Individual Access and ability to use an Apple iPhone® compatible with Medtronic's research app (iOS® v. 13.X or higher)
* Patient is willing and able to comply with the protocol, including CareLink transmissions (requires adequate connectivity), remotely administered instructions, and remote survey participation
* Patient is 22 years of age or older
* Located in the United States, with CareLink managed through servers located in United States (50 states or District of Columbia)
* Valid email address from self-report at enrollment
* Patient must be able to read and write in English
Exclusion Criteria Patients with \> 24 months elapsed time from recorded LINQ device implant or \> 48 months elapsed from recorded LINQ II implant date
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
22 Years
Study:
NCT04926857
Study Brief:
Protocol Section:
NCT04926857