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PAtient NOtifier Feature for Reduction of Anxiety

NCT00559559 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 362

Last updated 2019-02-04

No results posted yet for this study

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

  • Tachycardia, Ventricular

Interventions

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.

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Principal Investigators

  • Firat Duru, Prof. · Universitätsspital Zürich

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2010-12-31
Completion
2010-12-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00559559 on ClinicalTrials.gov