K62.3
Conditions
Interventions
Group 1: Data collection takes place at three defined points in time: preoperatively and 6 months and 12 months after resection rectopexy.
The first data collection involves providing information and
Sponsors
Klinik für Algemein- und Viszeralchirurgie- Universitätsklinikum Ulm
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Indication for prolapse surgery for grade I-V rectal prolapse according to Oxford classification Minimally invasive robotic surgery Verbal and written consent Ability to understand the content and scope of the study and to implement it
Exclusion criteria
Exclusion criteria: Incapacity to consent Age < 18 years Life expectancy < 12 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The difference in overall quality of life measured using the EORTC QLQ-C30 before resection rectopexy and 6 months postoperatively. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Quality of life 12 months postoperatively - Quality of life taken from additional questionnaires: EORTC QLQ-CR29, FIQoL - Outcome: Constipation based on CCCS, incontinence based on CCIS, patient satisfaction based on FIPS, postoperative complications, rate of anastomotic leakage, length of hospital stay | — |
Countries
Germany
Contacts
Public ContactMarko Kornmann
Klinik für Algemein- und Viszeralchirurgie- Universitätsklinikum Ulm
Outcome results
None listed