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.