Feasibility Study of Remote Support for Implantable Pulse Generator (IPG)/Implantable Cardioverter Defibrillator (ICD) Implant
| Status: | Completed |
|---|---|
| Conditions: | Cardiology |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 5/3/2014 |
| Start Date: | December 2013 |
| End Date: | March 2014 |
| Contact: | Reece Holbrook, BSEE |
| Email: | medtroniccrmtrials@medtronic.com |
| Phone: | 763-526-2772 |
Remote Implant Support
The purpose of this study is to gain real world, live implant experience with the remote
implant support system. This system is intended to provide the technical support for device
implants from a remote location through telepresence (audio and video) and remote control.
Specifically, the goals of this study are to corroborate bench testing, assess the
performance of the system, gain understanding of the workflows, customer experience, and
logistics.
The intent of the remote support model is to provide the same support that would typically
be provided by a local support person, only remotely. As such, the remote support person
would only perform actions that a local support person would routinely do under the
direction of a physician. This may involve observing patient data, providing technical
support and advice, and performing testing and device reprogramming via remote control of
the programmer.
implant support system. This system is intended to provide the technical support for device
implants from a remote location through telepresence (audio and video) and remote control.
Specifically, the goals of this study are to corroborate bench testing, assess the
performance of the system, gain understanding of the workflows, customer experience, and
logistics.
The intent of the remote support model is to provide the same support that would typically
be provided by a local support person, only remotely. As such, the remote support person
would only perform actions that a local support person would routinely do under the
direction of a physician. This may involve observing patient data, providing technical
support and advice, and performing testing and device reprogramming via remote control of
the programmer.
Inclusion Criteria:
- Planned IPG implant or planned ICD (without CRT) implant
- Signed informed consent
Exclusion Criteria:
- Pacing dependency
- Defibrillation threshold testing planned
- Basal ventricular rate >110 beats per minute
- Younger than 18 years
- Pregnant
- Currently involved in another IPG or ICD related clinical trial
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