Remote Interrogation in Rural Emergency Departments
Withdrawn before enrolling · Phase 4
Conditions studied: Heart Disease, Cardiovascular Disease, Heart Failure, Arrhythmias, Cardiac
In brief
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.
Key facts
- Study ID
- NCT02421549
- Run by
- Abbott Medical Devices
- People needed
- 0
- Starts
- 2014-12-01
- Expected to finish
- 2016-01-01
- Last updated by the study team
- 2019-02-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Presents to Emergency Department with an implanted pacemaker or defibrillator.
- Are 18 years of age or older.
- Are willing and able to provide informed consent for study participation.
- Are willing and able to complete a 30-60 day follow up phone call.
You may not qualify if…
- Are unwilling to provide written informed consent.
Where it is running
- New Mexico Heart Institute — Albuquerque, New Mexico, United States
Full record on ClinicalTrials.gov
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