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  3. NCT05210738

Single-incision Sling vs Urethral Bulking During Prolapse Surgery for Occult Stress Incontinence

Stress Incontinence, Female Clinical Trial

Official title:
A Cohort Observational Study Comparing the Outcomes of Single-incision Sling vs Urethral Bulking During Prolapse Surgery for Occult Stress Incontinence

Clinical Trial Summary

The aim is to compare outcomes of two different procedures to prevent occult stress urinary incontinence (SUI) in patients who are having pelvic organ prolapse surgeries

Clinical Trial Description

The aim is to compare outcomes of two different procedures to prevent occult stress urinary incontinence (SUI) in patients who are having pelvic organ prolapse surgeries. Charts will be reviewed for patients who had single- incision sling or urethral bulking injection with other prolapse surgeries to address occult stress incontinence at The Christ Hospital from the period of January 2019 to June 2021. Patients who didn't have any occult stress incontinence pre-operatively and didn't receive any anti-incontinence procedure during their prolapse surgery will be included as a control group. Surgical details, adverse events and postoperative voiding times will be collected from the chart. Patients will be contacted by a telephone to administer a validated questionnaire; a 3-day bladder diary to quantify urinary incontinence will be send to the patient to complete and return by mail. The purpose of the study is to investigate whether urethral bulking is as effective as single- incision sling in treating occult stress incontinence. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05210738
Study type Observational
Source The Christ Hospital
Contact
Status Completed
Phase
Start date January 1, 2019
Completion date June 1, 2021
View Details
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