Urinary Incontinence Clinical Trials

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Development and Validation of a Risk Prediction Model for De Novo Stress Urinary Incontinence After Pelvic Floor Reconstruction Surgery: A Case-Control Study

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

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
Participation Requirements
Sex: Female
Minimum Age: 20
Maximum Age: 90
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
China
Shanghai General Hospital
RECRUITING
Shanghai
Contact Information
Primary
Yiping Zhu
zhuypurologist@163.com
+86 13817665076
Time Frame
Start Date: 2024-12-01
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 382
Sponsors
Leads: Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

This content was sourced from clinicaltrials.gov