Extended Ambulatory Monitoring Improves Risk Stratification in

Status Active, not recruiting

Clinical Trial Summary

Eligible subjects will wear 4 consecutive external monitoring devices for a total of 28 days of monitoring.

Clinical Trial Description

Eligible subjects will be monitored with a SEEQ device. The SEEQ device is a patch-like device that is worn externally on the chest and continuously monitors heart rhythm. Each device is worn for seven days and replaced with additional devices for a total of 28 days of monitoring. Subjects will return the SEEQ equipment at the end of the monitoring period. Subjects will be contacted by telephone or seen at the clinic approximately 60 days from the first day of monitoring. Information will be gathered about medications and any cardiac interventions the subject may have had.

Subjects will again be contacted by telephone or seen in the clinic approximately 1 year from study start. Information will be gathered about general health, changes in medications, and cardiac interventions or events. Cardiac testing results will be reviewed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03182153
Study type	Observational
Source	Atlantic Health System
Contact
Status	Active, not recruiting
Phase
Start date	November 2016
Completion date	December 31, 2018

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Extended Ambulatory Monitoring Improves Risk Stratification in Hypertrophic Cardiomyopathy

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms