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.
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.
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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