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Urethral Length Measurement in Women Undergoing Suburethral Sling Operative Procedure

Stress Urinary Incontinence Clinical Trial

Official title:
Prospective, Non-randomized, Observational Study of the Surgical Management of Suburethral Slings in Women With Stress Urinary Incontinence

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01660438
Study type Observational
Source Cantonal Hospital, Frauenfeld
Contact
Status Completed
Phase N/A
Start date August 2010
Completion date February 2013
View Details
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