Cardiac Monitor Employee Study

Last updated: July 3, 2019
Sponsor: Boston Scientific Corporation
Overall Status: Completed

Phase

N/A

Condition

Circulation Disorders

Treatment

N/A

Clinical Study ID

NCT03826225
CARMEL
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

This purpose of this study is to collect ECG data from a wearable cardiac monitor in order to evaluate end-to-end performance of a cardiac monitor system and associated data management accessories.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Willing and capable to provide informed consent

  • Age 18 or above

  • Employee of the study sponsor

  • Willing and able to follow protocol requirements

Exclusion

Exclusion Criteria:

  • Currently enrolled in another clinical study that interferes with data collection

  • Currently implanted with an active medical electronic device

  • Known allergies to the materials that may come in contact with the skin

  • Any active skin condition on the chest reported by the subject

Study Design

Total Participants: 20
Study Start date:
March 07, 2019
Estimated Completion Date:
May 23, 2019

Study Description

The objective of this study is to evaluate the usability of the Wearable Cardiac Monitor (WCM) system including the WCM, Mobile Monitors (patient and clinician), Magnet and LATITUDE Clarity(TM) Server. The study will exercise the end-to-end system utilizing human ECG data generated by the wearable cardiac monitor.

Connect with a study center

  • Boston Scientific

    Saint Paul, Minnesota 55112
    United States

    Site Not Available

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.