The CUPIDO-3. A diagnostic study to evaluate barrier tests in predicting postoperative stress incontinence in women with genital prolapse.

The CUPIDO-3. A diagnostic study to evaluate barrier tests in predicting postoperative stress incontinence in women with genital prolapse. - Barrier test study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON31808

Enrollment

120

Registered

2008-09-08

Start date

2008-02-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

genital prolaps pelvic organ prolapse

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Women of 18 year and older planned for vaginal repair of genital prolaps

Exclusion criteria

Exclusion criteria: Mental handicap or unable to to provide informed consent or to complete testing or data collection. Pregnancy by self-report or positive pregnancy test, or self-reported intention to become pregnant. 12 months or less postpartum (defined as delivery or other termination after 20 wk). Prior surgery for urinary incontinence (eg TVT or Burch). Recent (

Design outcomes

Primary

Measure	Time frame
absence of urinary (stress) incontinence and subsequent treatment for urinary (stress) incontinence at 6 and 12 months	—

Secondary

Measure	Time frame
Urinary distress at 6 and 12 months measured with validated Dutch UDI questionnaire	—

Countries

Netherlands

Outcome results