vault prolapse
Conditions
Interventions
INTERVENTIONS: Open abdominal sacral colpopexy versus laparoscopic sacral
colpopexy
Sponsors
Máxima Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: All hysterectomised patients with a vaginal vault prolapse are elegible for the study.
Exclusion criteria
Exclusion criteria: Patients with a contraindication for a surgical intervention will be excluded
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| OUTCOME MEASURES: The primary outcome will be quality of life. The urogenital distress inventory (UDI) will be the quality of life measure in this trial. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome will be women*s perceived improvement in the prolapse symptoms and clinicians post-operative grading of prolapse until one year of follow-up, costs and cost-effectiveness. | — |
Countries
Netherlands
Outcome results
None listed