Trials / Completed
CompletedNCT00559559
PAtient NOtifier Feature for Reduction of Anxiety
PAtient NOtifier Feature for Reduction of Anxiety: A Multicenter ICD Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 362 (actual)
- Sponsor
- Abbott Medical Devices · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is intended to look at the effect of the SJM vibrating Patient Notifier™ system, which will warn the patient of possible failures of the implanted system, on reducing patient device related anxiety
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ICD implant + Patient Notifier turned OFF | ICD implant, plus standard care, i.e. Patient Notifier turned off |
| PROCEDURE | ICD Implant + Patient Notifier turned ON | ICD implant. The Patient Notifier™ feature will be turned ON. |
Timeline
- Start date
- 2007-12-01
- Primary completion
- 2010-12-01
- Completion
- 2010-12-01
- First posted
- 2007-11-16
- Last updated
- 2019-02-04
Locations
1 site across 1 country: Switzerland
Source: ClinicalTrials.gov record NCT00559559. Inclusion in this directory is not an endorsement.