I34.0
Conditions
Interventions
Group 1: Comparison of measurements obtained using perioperative 2D echocardiography (TEE) with the size of the implanted annuloplasty ring. For all included patients, echocardiographic measurements
Sponsors
Universitätsklinikum Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients > 18 years old, male or female Surgical mitral valve repair Use of 3D-software
Exclusion criteria
Exclusion criteria: Obesity (BMI > 40) No preoperative echocardiographic findings available Poor image quality (TEE) Endocarditis of the mitral valve History of interventional mitral valve procedure Emergency surgeries Reoperation on the mitral valve
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| For all included patients, echocardiographic measurements will be collected once prior the start of the surgery. The primary endpoints are correlations between the following measurements and the size of the implanted annuloplasty ring: 1. 2D measurements - AP diameter - Intercommissural diameter 2. 3D measurements - AP diameter - AL-PM diameter | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlations of additional measurements obtained through a 3D-software with the size of the implanted annuloplasty ring Correlations of additional measurements obtained using 2D echocardiography with the size of the implanted annuloplasty ring Correlations of measurements obtained using 3D echocardiography with subsequent processing in MPR (multiplanar reconstruction) with the size of the implanted annuloplasty ring | — |
Countries
Germany
Contacts
Public ContactFelix Ulbrich
UHZ Freiburg-Bad Krozingen
Outcome results
None listed