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:
2025-12-25 @ 1:40 AM
Ignite Modification Date:
2025-12-25 @ 1:40 AM
NCT ID:
NCT02162394
Eligibility Criteria:
Inclusion Criteria:
* Patients must be at least 18 years of age
* Patients must have a medical indication to wear a Holter monitor
* Patients must not be pregnant
* Patients must be able to comply with the study procedures
* Patients must be willing to participate and able to provide informed consent
* Patients must be willing to wear both devices (Holter and the wireless device prototype) simultaneously and continuously for a 2 to 3 hr period
Exclusion Criteria:
* Patients who are not able or willing to comply with study procedures
* Patients with an existing implanted cardioverter-defibrillator and/or pacemaker
* Patients with a known life threatening arrhythmia
* Patients who manifest low voltage on their electrocardiogram
* Patients affected by inflammatory and/or infectious skin disorders
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02162394
Study Brief:
Protocol Section:
NCT02162394