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ClinicalTrials.gov ID

NCT07628036

Lead Sponsor

Hospital Universitari Vall d'Hebron Research InstituteOTHER

Overall Status

Not yet recruiting

Study Type

Observational

Enrollment

1,042Estimated

Last Update Posted

Jun 4, 2026Actual

Start Date

Aug 1, 2026Estimated

Primary Completion Date

May 30, 2028Estimated

Completion Date

May 30, 2028Estimated

Official Title

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

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.

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

• Vaginal surgery for pelvic organ prolapse

Ages Eligible for Study

Adult (18-64)Older Adult (65+)

Sexes Eligible for Study

Female

Accepts Healthy Volunteers

No

Eligibility Criteria

Inclusion Criteria:

• Women who will undergo vaginal surgery for pelvic organ prolapse

Exclusion Criteria:

• inhability to give consent to the study

Observational Model

Cohort

Time Perspective

Prospective

Lead Sponsor

Hospital Universitari Vall d'Hebron Research InstituteOTHER

Collaborators

University Hospital Virgen de la Arrixaca, MurciaUNKNOWN

Hospital Materno-Infantil de Canarias. Las Palmas de Gran Canaria. SpainUNKNOWN

Hospital de l'Esperit SantUNKNOWN

Consorci Sanitari de TerrassaOTHER

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