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Resorbable Magnesium Scaffolds Registry
Sponsor: Biotronik AG
Summary
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).
Official title: RMS (Resorbable Magnesium Scaffolds) Registry
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
1106
Start Date
2020-11-18
Completion Date
2030-05
Last Updated
2025-11-21
Healthy Volunteers
No
Conditions
Interventions
Magmaris
MAGMARIS is indicated for improving luminal diameter in the treatment of de novo native coronary artery lesions in patients with symptomatic coronary artery disease. The reference vessel diameter should closely match the scaffold nominal diameter. The treated lesion length should be less than the nominal scaffold length.
Freesolve
Freesolve is indicated for improving luminal diameter in the treatment of de novo native coronary artery lesions in patients with symptomatic coronary artery disease. The reference vessel diameter should closely match the scaffold nominal diameter. The treated lesion length should be less than the nominal scaffold length.
Locations (13)
Cairns Hospital
Cairns, Australia
Heart Center Segeberger Kliniken
Bad Segeberg, Germany
Krankenhaus Buchholz
Buchholz, Germany
Klinikum Westfalen, Knappschaft KH
Dortmund, Germany
Klinikum Herford
Herford, Germany
Herz-und Gefäßzentrum Oberallgäu-Kempten
Kempten, Germany
Centro Cardiologico Monzino
Milan, Lombardy, Italy
Daugavpils Regional Hospital
Daugavpils, Latvia
1 Wojskowy Szpital Kliniczny z Poliklinika SPZOZ w Lublinie
Lublin, Poland
SUSCCH Banska Bystrica
Banská Bystrica, Slovakia
Lindenhofspital
Bern, Switzerland
Centre Hospitalier Universitaire Vaudois
Lausanne, Switzerland
Solothurner Spitäler AG
Olten, Switzerland