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

Use our guide to learn which trials are right for you!

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).


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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Oklahoma City, OK
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from
Aurora, CO
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from
Clearwater, FL
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from
Jackson, MS
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from
Jacksonville, FL
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mi
from
Larkspur, CA
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mi
from
Las Vegas, NV
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Palm Beach Gardens, Florida 33410
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mi
from
Palm Beach Gardens, FL
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mi
from
Palo Alto, CA
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mi
from
Rome, GA
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mi
from
Sacramento, CA
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mi
from
Sebring, FL
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mi
from
Simi Valley, CA
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mi
from
The Woodlands, TX
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mi
from
Youngstown, OH
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