Remote Interrogation in Rural Emergency Departments
| Status: | Withdrawn |
|---|---|
| Conditions: | Peripheral Vascular Disease, Cardiology, Hospital |
| Therapuetic Areas: | Cardiology / Vascular Diseases, Other |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 2/6/2019 |
| Start Date: | December 2014 |
| End Date: | January 2016 |
Remote Interrogation of Implantable Cardiac Devices in Rural Emergency Departments
A retrospective, multi-center, proof-of-concept study to evaluate the use of remote
monitoring in rural emergency departments to decrease time to treatment decision for
pacemaker and defibrillator patients using the St Jude Medical Merlin@home transmitter. The
purpose of the study is to determine if utilization of remote monitoring technology in a
rural emergency department may improve patient care.
Up to 10 rural ED sites will enroll a total of 200 patients. One hundred patients will be in
the remote monitoring group comprised of patients with SJM devices compatible with the
unpaired transmitter and 100 patients will be in the usual medical care group comprised of
patients with SJM devices that are not compatible with the unpaired transmitter or that have
a competitor's device.
monitoring in rural emergency departments to decrease time to treatment decision for
pacemaker and defibrillator patients using the St Jude Medical Merlin@home transmitter. The
purpose of the study is to determine if utilization of remote monitoring technology in a
rural emergency department may improve patient care.
Up to 10 rural ED sites will enroll a total of 200 patients. One hundred patients will be in
the remote monitoring group comprised of patients with SJM devices compatible with the
unpaired transmitter and 100 patients will be in the usual medical care group comprised of
patients with SJM devices that are not compatible with the unpaired transmitter or that have
a competitor's device.
Inclusion Criteria:
1. Presents to Emergency Department with an implanted pacemaker or defibrillator.
2. Are 18 years of age or older.
3. Are willing and able to provide informed consent for study participation.
4. Are willing and able to complete a 30-60 day follow up phone call.
Exclusion Criteria:
1. Are unwilling to provide written informed consent.
We found this trial at
1
site
Click here to add this to my saved trials
