Clinical Trials Directory

Trials / Completed

CompletedNCT01526629

Full Automaticity and Remote Follow-up

Identification of Implantable Cardioverter Defibrillator Patients With Remote Follow up That Requires an Onsite Visit

Status
Completed
Phase
Study type
Observational
Enrollment
354 (actual)
Sponsor
Medtronic Cardiac Rhythm and Heart Failure · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

With the expansion of Sudden Cardiac Death (SCD) primary prevention indications, the number of Implantable Cardioverter Defibrillators (ICD) implants has increased significantly in the recent years. This has resulted in an increase of the number of follow-up (FU) to be performed and a growing workload for centers. Remote FU system such as the Medtronic Carelink system allows to check remotely the proper functioning of self evaluating devices and give informations of some clinical events. The objective of this study is to define which patients with a remote follow-up need additional onsite visit and to assess to which extent remote FU can be an alternative to onsite visit.

Conditions

Timeline

Start date
2011-05-01
Primary completion
2015-03-01
Completion
2015-03-01
First posted
2012-02-06
Last updated
2025-07-02
Results posted
2017-06-29

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01526629. Inclusion in this directory is not an endorsement.