Development and Validation of a Risk Prediction Model for De Novo Stress Urinary Incontinence After Pelvic Floor Reconstruction Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age20-90
SponsorShanghai General Hospital, Shanghai Jiao Tong University School of Medicine

About this trial

This observational study aims to develop a predictive model for the occurrence of new-onset stress urinary incontinence (SUI) after pelvic organ prolapse (POP) repair surgery in women. The primary questions it seeks to answer are:

Which risk factors and anatomical characteristics predispose women to new-onset stress urinary incontinence following pelvic organ prolapse repair surgery?

Female POP patients without any preoperative symptoms of urinary incontinence will receive telephone follow-ups at 3, 6, and 12 months after undergoing standard surgical treatment.

Eligibility criteria

Qualifiers

Patients with pelvic organ prolapse quantification (POP-Q) stage II or higher;

Patients who require surgical treatment for pelvic organ prolapse;

Patients with no evidence of urinary incontinence before surgery.

Disqualifiers

Patients confirmed to have urinary incontinence before surgery;

Patients with urinary or reproductive system infections;

Patients with a history of prior surgery for urinary incontinence;

Patients who have undergone previous mesh repair surgery for pelvic organ prolapse;

Trial design

Treatments tested in this trial

  • Telephone follow-up

Treatment groups

No treatment groups listed