Observation of Clinical Routine Care for Patients With BIOTRONIK Implantable Cardiac Monitors (ICMs)

Recruiting Observational Study
Tachycardia Atrial Fibrillation Syncope Bradycardia Cryptogenic Stroke
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
1,400 (estimated)
Sponsor
Biotronik SE & Co. KG · Industry
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About This Trial
This registry is performed for the long-term assessment of outcome, performance and residual safety aspects of the BIOMONITOR III and possible successors in a real-life clinical set-up. In addition, this registry is set up in a way that it may also be used as a platform for submodules to investigate additional scientific and regulatory aspects while minimizing the additional effort for the investi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patient is intended to receive a BIOTRONIK Implantable Cardiac Monitor (ICM) * Patient is able to understand the nature of the registry and to provide written informed consent. * Patient is willing and able to use the CardioMessenger and accepts the BIOTRONIK Home Monitoring c…
Contacts

Sabrina Hoche, Dr.

+49 30 68905

biomonitor-registry@biotronik.com

CONTACT

Dörte Vossmeyer, Dr.

+49 30 68905

biomonitor-registry@biotronik.com

CONTACT