Clinical Trials Directory

Trials / Completed

CompletedNCT04981054

BO and DO in Women With Cystocele Before and After Cystocele Repair

Prevalence of Bladder Oversensitivity and Detrusor Overactivity in Women With Cystocele and the Changes of Storage Function After Cystocele Repair

Status
Completed
Phase
Study type
Observational
Enrollment
483 (actual)
Sponsor
National Taiwan University Hospital · Academic / Other
Sex
Female
Age
20 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The changes of lower urinary tract function after cystocele repair are important for perioperative consultation and management. Thus, the aim of this retrospective study was to evaluate the prevalence of bladder oversensitivity and detrusor overactivity in women with ≥ stage II cystocele and the changes of storage function after cystocele repair.

Detailed description

Bladder oversensitivity and detrusor overactivity are two important diagnosis of urodynamic study regarding storage function of bladder. Between November 2010 and October 2020, all women with ≥ stage II cystocele who visited the urogynecological department of a medical center for cystocele repair were reviewed. Those women who had complete data of preoperative and postoperative 3-month follow-up urodynamic data were excluded from this study. Bladder oversensitivity was diagnosed if the volume of strong desire was less than 300mL. Detrusor overactivity was defined as the occurrence of involuntary detrusor contractions during filling cytometry. STATA software was used for statistical analysis. Chi2 test, univariate and multivariable logistic regression tests were used for statistical analysis as appropriate. A p \< 0.05 was considered as statistically significant.

Conditions

Interventions

TypeNameDescription
PROCEDURECystocele repairRepair of endopelvic fascia and anterior colporrhaphy

Timeline

Start date
2010-11-01
Primary completion
2020-10-31
Completion
2020-10-31
First posted
2021-07-28
Last updated
2021-07-28

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT04981054. Inclusion in this directory is not an endorsement.