Trials / Completed
CompletedNCT01660438
Urethral Length Measurement in Women Undergoing Suburethral Sling Operative Procedure
Prospective, Non-randomized, Observational Study of the Surgical Management of Suburethral Slings in Women With Stress Urinary Incontinence
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 188 (actual)
- Sponsor
- Cantonal Hospital, Frauenfeld · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective, non-randomized, observational, multicenter study in which urethral length is measured in women with surgically-correctable stress urinary incontinence who undergo a suburethral sling operative procedure.
Detailed description
This is a prospective, non-randomized, observational, multicenter study in which urethral length is measured in women with surgically-correctable stress urinary incontinence who undergo a suburethral sling operative procedure. Data will be collected from preoperative urogynecological testing and medical histories. The urethral length will be measured intraoperatively using scaled catheters. Outcome data, including the development of postoperative complications, will be collected at several time intervals.
Conditions
Timeline
- Start date
- 2010-08-01
- Primary completion
- 2013-02-01
- Completion
- 2013-02-01
- First posted
- 2012-08-08
- Last updated
- 2016-05-20
Locations
3 sites across 3 countries: Germany, Poland, Switzerland
Source: ClinicalTrials.gov record NCT01660438. Inclusion in this directory is not an endorsement.