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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03613350
Other study ID # 201805024RINB
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2011
Est. completion date May 31, 2018

Study information

Verified date July 2018
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Prevalence rates of urodynamic stress incontinence (USI), bladder oversensitivity (BO) /detrusor overactivity (DO) or both and their related clinical and urodynamic findings in women with ≥ pelvic organ prolapse quantification stage II cystocele are important for clinical consultation. Thus, the aim of this study was to elucidate the above findings and between-group associations.


Description:

Between November 2011 and January 2017, medical records of all women with ≥stage II cystocele who underwent 20-minute pad testing and urodynamic studies in a medical center were reviewed. ANOVA test and post-hoc testing with bonferroni's correction were used for statistical analysis. USI included evident USI and occult USI, which were classified according to pad weight before and after prolapse reduction. BO was defined as <300 mL of the volume at strong desire to void during filling cystometry. Those women without USI, BO or DO were allocated into the no demonstrated USI+BO/DO group.


Recruitment information / eligibility

Status Completed
Enrollment 480
Est. completion date May 31, 2018
Est. primary completion date January 31, 2017
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

1. Age >20y/o

2. Severe cystocele, ie, more than stage 2

3. Complete pad test and urodynamic study

Exclusion Criteria:

1. Pregnancy

2. Urinary tract infection

3. Had received pelvic reconstruction

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Pad test
20-minutes pad test and urodynamic study (including uroflowmetry, filling and voiding cystometry, and urethral pressure profile) were conducted to every patient.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary USI Urodynamic stress incontinence was noted during examination Between November 2011 and January 2017
Primary BO/DO Bladder oversensitivity/detrusor overactivity was noted during examination Between November 2011 and January 2017