SEEQ™ Performance Study
Status: | Recruiting |
---|---|
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | June 2015 |
End Date: | September 2016 |
Contact: | SEEQ™ Performance Study Clinical Team |
Email: | medtronicCRMtrials@medtronic.com |
Phone: | 1-800-328-2518 |
The purpose of the Medtronic SEEQ™ Performance study is to build further evidence on the
clinical and economic benefit of the Medtronic market-released SEEQ™ Mobile Cardiac
Telemetry System/External Cardiac Monitor System (MCT/ECM).
clinical and economic benefit of the Medtronic market-released SEEQ™ Mobile Cardiac
Telemetry System/External Cardiac Monitor System (MCT/ECM).
Inclusion Criteria:
- Patient is indicated for a SEEQ™ MCT/ECM System for approved indications
- Patient is 18 years of age or older
- Patient is willing and able to provide consent and authorize the use and disclosure
of health information
- Patient is willing and able to comply with the protocol
Exclusion Criteria:
- Patient has known allergy and/or hypersensitivity to adhesives or hydrogel.
- Patient has suspected potential life-threatening arrhythmias, or requires
in-subject/in-hospital monitoring.
- Patient will undergo a medical procedure that would preclude full participate during
the prescribed duration of the SEEQ™
- Patient has an implanted cardiac device, (e.g., pacemaker, Implantable Cardioverter
Defibrillator, Cardiac Resynchronization Therapy)
We found this trial at
15
sites
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