Study cohort: cardiac surgeons I34.0
Conditions
Interventions
Group 1: Various cardiac surgeons from different countries and/or different hospitals will perform mitral valve reconstruction on patient-specific pathological silicone mitral valves (duration: approx
Sponsors
Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Cardiac surgeons (m/f/d) with mitral valve reconstruction experience
Exclusion criteria
Exclusion criteria: Absence of signed informed consent or withdrawal request.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quantification of the surgical outcome in a hemodynamic simulator, for example by measuring the regurgitant volume. Comparison before and after the operation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Intraoperative decisions, such as the choice of surgical technique, which may vary depending on the situation. | — |
Countries
Belgium, Czechia, Germany, Netherlands, Spain
Contacts
Public ContactSandy Engelhardt
Universitätsklinikum Heidelberg
Outcome results
None listed