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Study identifier: NCT04241328 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery

Condition: Cardiovascular Diseases  ·  Sponsor: Medtronic Cardiac Surgery

PhaseN/A
Planned participants5000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Lisa Lindelauf, BSc  ·  +31611605434  ·  lisa.lindelauf@medtronic.com

Always discuss trial participation with your own doctor first.

Locations (14)

AKH WienVienna, AustriaRecruiting
Ziekenhuis Oost-LimburgGenk, BelgiumRecruiting
UZ LeuvenLeuven, BelgiumRecruiting
CHU d'AngersAngers, FranceCompleted
Clinique Claude BernardMetz, FranceTerminated
Uniklinik RWTH AachenAachen, GermanyRecruiting
Herz- und Diabeteszentrum NRWBad Oeynhausen, GermanyRecruiting
Deutsches Herzzentrum MünchenMunich, GermanyRecruiting
Onassis HospitalAthens, GreeceActive Not Recruiting
Catharina ZiekenhuisEindhoven, NetherlandsCompleted
Maastricht University Medical Center (MUMC+)Maastricht, NetherlandsActive Not Recruiting
St. Antonius ZiekenhuisNieuwegein, NetherlandsRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT04241328