I21
Conditions
Interventions
Group 1: STEMI DESolve (bioresorbable vascular scaffolds (BRS) in Patient with ST-Segment myocardial Infarction (STEMI). Every Patient with STEMI and BRS is enrolled in the study. Additional the Patie
Sponsors
Universitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: -All Patients with STEMI and with a anatomically suitable coronarstatus -Written agreement of the Patient
Exclusion criteria
Exclusion criteria: -Intellectual reduction, No suitable coronarstatus (ostial leasion, bifurcation, calc rich leasions)
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| -TIMI 0, I, II, III Fluss -Angina Pectoris -Successfull Stent-Implantationen -Target vessel failure (cardiac death, target vessel MI, or clinically driven target vessel revascularisation (TVR), and scaffold thrombosis (ST)) -Kidneyinjury -Rhythm-Events | — |
Primary
| Measure | Time frame |
|---|---|
| device-oriented composite endpoint within 36 Month (target lesion failure [TLF]), defined as the combination of cardiac death, target vessel MI, or clinically driven target lesion revascularisation (TLR), either percutaneous or surgical. Deaths that could not be attributed to another cause were re-garded as cardiac deaths. OCT subgroup: neointima formation after 4-6 month | — |
Countries
Germany
Contacts
Public ContactFelix Hauptmann
Brüderkrankenhaus Trier
Outcome results
None listed