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Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery

Recruitingn/aAges any - anyAllMedtronic Cardiac Surgery
NCT04241328 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The purpose of this observational, multi-center prospective, post-market registry is to confirm real-world device safety and performance, to ensure the continued acceptability of identified risks, and detect emerging risks.

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: * Subject or legally authorized representative provides written data release and/or informed consent per institution and/or geographical requirements prior to discharge from participating registry hospital. * Subject will undergo or underwent a procedure in which an eligible Medtronic CS product is/was used. Exclusion Criteria: * Currently participating in an interventional drug or device study which may induce confounding factor(s) to the results from this Registry
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What it tests

  • Not listed
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Where

14 sites
AKH Wien
Vienna, Austria
Ziekenhuis Oost-Limburg
Genk, Belgium
UZ Leuven
Leuven, Belgium
CHU d'Angers
Angers, France
Clinique Claude Bernard
Metz, France
Uniklinik RWTH Aachen
Aachen, Germany
Herz- und Diabeteszentrum NRW
Bad Oeynhausen, Germany
Deutsches Herzzentrum München
Munich, Germany

…and 6 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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