Urinary Continence After Vaginal Surgery for Genital Prolapse in the Spanish Population.

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07628036

Enrollment

1042

Registered

2026-06-04

Start date

2026-08-01

Completion date

2028-05-30

Last updated

2026-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Organ Prolapse (POP), Pelvic Organ Prolapse Vaginal Surgery, Urinary Incontinence (UI)

Keywords

Pelvic organ prolapse, Vaginal surgery, Urinary incontinence, Stress urinary incontinence, Urge-urinary incontinence

Brief summary

Surgical correction of pelvic organ prolapse (POP) may be associated with the development of postoperative stress urinary incontinence (SUI). This clearly affects women's satisfaction and their quality of life, and may require subsequent medical and/or surgical treatments. On the other hand, pre-existing SUI could resolve after corrective prolapse surgery. Similarly, urge urinary incontinence (UUI) could appear or improve after vaginal POP surgery. Therefore, it is of paramount importance to know the prevalence of urinary incontinence after POP vaginal surgery and incontinence resolution in our population. Identifying the risk factors for the development of urinary incontinence may allow to provide individualized treatment.

Interventions

PROCEDUREVaginal surgery for pelvic organ prolapse

Vaginal surgery of any vaginal compartment for pelvic organ prolapse

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 99 Years

Healthy volunteers

Inclusion criteria

* Women who will undergo vaginal surgery for pelvic organ prolapse

Exclusion criteria

* inhability to give consent to the study

Design outcomes

Primary

Measure	Time frame
Stress urinary incontinence (SUI).	1 year after surgery.
Urgency urinary incontinence (UUI)	1 year after surgery

Secondary

Measure	Time frame
Incontinence severity	1 year after surgery
Patient's satisfaction with the procedure.	1 year after surgery

Countries

Spain

Contacts

CONTACTJordi Sabadell, MD, PhD

jordi.sabadell@vallhebron.cat+34934894010

PRINCIPAL_INVESTIGATORSabadell Jordi, MD, PhD.

Hospital Universitari Vall d'Hebron Research Institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 5, 2026