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Clinical Trials/ACTRN12607000517471
ACTRN12607000517471
Active, not recruiting
未知

The ACQUIRE Study: To assess the impact of remote device follow-up on time and financial burden in patients with a pacemaker, implantable cardioverter defibrillator or cardiac resynchronisation therapy device.

Medtronic Australasia Pty Ltd0 sites225 target enrollmentOctober 9, 2007

Overview

Phase
未知
Intervention
Not specified
Conditions
Remote monitoring of implanted cardiac devices: Pacemaker, Implantable Cardioverter Defibrillator (ICD) or cardiac resynchronisation therapy (CRT) device
Sponsor
Medtronic Australasia Pty Ltd
Enrollment
225
Status
Active, not recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 9, 2007
End Date
TBD
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patient is scheduled to receive (or has a previously implanted) IPG, ICD or CRT device that is supported by the Medtronic CareLink Network.
  • Patient has access to a telephone line where they reside, and are willing and able to use the Medtronic CareLink Monitor and perform the required duties at home or have a family member or assistant perform those duties.
  • Patient signs the study consent form and agrees to comply with all study requirements

Exclusion Criteria

  • Patient is enrolled in, or intends to participate in, another clinical trial that might conflict with this study.
  • Patient has medical conditions that would limit study participation (e.g. hearing or speech impaired with no family member or assistant available).

Outcomes

Primary Outcomes

Not specified

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