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NCT04412928 Clinical Trial

Factors Affecting the Cure of Overactive Bladder Syndrome in Women Underwent Mid-urethral Sling Procedure

Stress Urinary Incontinence Clinical Trial

Official title:
Factors Affecting the Cure of Overactive Bladder Syndrome in Women Underwent Mid-urethral Sling Procedure

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04412928
Other study ID # 109048-E
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 13, 2020
Est. completion date April 20, 2021

Study information
Verified date September 2023
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

We will estimate the incidence of patients with overactive bladder syndrome after surgery and explore related predictors.

Description:

At present, around 30% of women with stress urinary incontinence have overactive bladder syndrome after mid-urethral sling procedure. But its predictive factor is still unclear. We will estimate the incidence of patients with overactive bladder syndrome after surgery and explore related predictors. In addition, we will explore the cure rate and predictors of cure of overactive bladder syndrome after the mid-urethral sling procedure for women with stress urinary incontinence. The above results will be used as a reference for preoperative and postoperative consultation.

Recruitment information / eligibility
Status Completed
Enrollment 591
Est. completion date April 20, 2021
Est. primary completion date March 12, 2021
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria: - All women with stress urinary incontinence who underwent mid-urethral sling procedure from January 01, 2008 to July 31, 2019 will be reviewed. Exclusion Criteria: - Patients undergoing other gynecological operations at the same time, except for cystoscopy.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• mid-urethral sling procedure
mid-urethral sling procedure

Locations
Country Name City State
Taiwan Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital Banqiao New Taipei

Sponsors (1)
Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Factors affecting the presence of overactive bladder syndrome after mid-urethral sling procedure 10 year
Secondary Factors affecting cure of overactive bladder syndrome after mid-urethral sling procedure 10 years
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