sacrocolpopexy sacral colpopexy pelvic organ prolapse vault prolapse sacrocolpopexie prolaps vaginatopprolaps verzakking
Conditions
Interventions
Since this is a follow-up study, no interventions will be done.
Patiente are asked to fill out a questionnaire and to come to the out patient clinic once for a physical examination using POP-Q classi
Sponsors
Máxima Medical Centre, Veldhoven
Eligibility
Inclusion criteria
Inclusion criteria: - All patients from the original SALTO trial. - Willing to participate
Exclusion criteria
Exclusion criteria: - Died patients - Unwilling to participate. - Unable to visit the outpatient clinic.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this follow-up study is to evaluate long term outcome in terms of disease specific quality of life of the patient population of the SALTO1 trial. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objective of this follow-up study is to evaluate long term outcome in terms of patient’s subjective satisfaction, general quality of life, sexual functioning, subjective and objective recurrence, type and number of re-interventions and mesh and suture erosion in the patient population of the SALTO1 trial. | — |
Contacts
Public ContactMarlies Bongers
Máxima Medisch Centrum, Locatie Veldhoven, P.O. Box 7777
Outcome results
None listed