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

Recruitingn/aAges 18 Years - anyAllBiotronik SE & Co. KG
NCT04075084 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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 investigational sites and patients.

Sign in to get the eligibility rules as simple questions to take to your doctor.

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📋 Eligibility rules (as published)
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 concept. Exclusion Criteria: * Patient is pregnant or breast feeding. * Patient is less than 18 years old. * Patient is participating in another interventional clinical investigation other than the submodules of BIO\|STREAM.ICM
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What it tests

  • Not listed
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Where

31 sites
Integral Health
Adelaide, Australia
Royal Adelaide Hospital
Adelaide, Australia
Nemocnice Ceske Budejovice, a.s.
České Budějovice, Czechia
Hôpital Saint-André
Bordeaux, France
Le Centre Hospitalier Universitaire de Brest (CHRU Brest)
Brest, France
Le Centre Hospitalier Universitaire de Caen (CHRU Caen)
Caen, France
Le Centre Hospitalier Universitaire de Tours (CHRU Tours)
Chambray-lès-Tours, France
Hôpital Gabriel Montpied
Clermont-Ferrand, France

…and 23 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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