N81
Conditions
Interventions
Group 1: Retrospective analysis of patient data regarding perioperative complications and satisfaction among those who underwent prolapse surgery at Ulm University Hospital from 2014 to 2021.
Sponsors
Universitätsfrauenklinik Ulm
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Operative therapy (OPS code 5-704...) vaginal prolapse surgeries without alloplastic material vs vaginal prolapse surgeries with alloplastic material vs laparoscopic/open sacrocolpopexy with alloplastic material
Exclusion criteria
Exclusion criteria: For patients who cannot be reached by phone and/or whose written consent form is not available, only the perioperative data from the electronic medical records will be collected retrospectively.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of treatment satisfaction, based on the Freiburg Patient Satisfaction Index, in the surgical therapy of genital prolapse depending on the surgical technique (alloplastic material versus autologous tissue). Evaluation of the complication rate and type of complication in the surgical therapy of genital prolapse depending on the surgical technique (alloplastic material versus autologous tissue). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary study objective is to examine the relationship between patient-dependent co-factors and the rate and type of complications. | — |
Countries
Germany
Contacts
Public ContactMiriam Deniz
Universitätsfrauenklinik Ulm
Outcome results
None listed