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Construction of a risk prediction model for urinary incontinence and adverse events after female pelvic organ prolapse repair surgery

Construction of a risk prediction model for urinary incontinence and adverse events after female pelvic organ prolapse repair surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110164
Enrollment
Unknown
Registered
2025-10-09
Start date
2025-10-15
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

stress urinary incontinence

Interventions

No stress urinary incontinence group:None

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: Women aged 40-90 (including those aged 40 and 90); The patient has undergone POP repair surgery in the past; The patient has undergone POP repair surgery for at least 12 months prior to follow-up; During the POP repair surgery, anti stress urinary incontinence surgery was not performed simultaneously.

Exclusion criteria

Exclusion criteria: The patient reported that the symptoms of stress urinary incontinence persisted for >= 3 months before surgery; When the preoperative bladder capacity of the patient is <= 300ml, urinary leakage was observed during coughing and Valsalva action stress testing; The patient's preoperative bladder capacity is less than 200ml (measured by catheterization or ultrasound); The patient has undergone anti stress urinary incontinence surgery in the past.

Design outcomes

Primary

MeasureTime frame
International Consultation on Incontinence Questionnaire;

Secondary

MeasureTime frame
Preoperative POP-Q grading;Postoperative POP-Q classification;preoperative urodynamic parameters;preoperative pelvic floor ultrasound parameters;postoperative pressure test results;

Countries

China

Contacts

Public ContactLv Aiming

Beijing Hospital

lvaiming1983@163.com+86 137 1663 3843

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026