Resorbable Magnesium Scaffolds Registry

Recruiting Observational Study
Coronary Artery Disease
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
1,106 (estimated)
Sponsor
Biotronik AG · Industry
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About This Trial

The registry follows the ESC/EACTS guideline and further investigates the clinical performance and short-term safety of RMS (Resorbable Magnesium Scaffolds) in a real world setting within the scope of its intended use without further (medical related) exclusion criteria according to their respective instructions for use (IFU).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * According to the IFU Exclusion Criteria: * According to the IFU
Contacts

Marina Gattiglio, Dr.

+41754295843

marina.gattiglio@teleflex.com

CONTACT