Prospective, Non-Randomized, Observational Trial of the Surgical Management for Suburethral Slings in Women With Stress Urinary Incontinence

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This is a prospective, non-randomized, observational, single center study in which subjects that have surgically-correctable Stress Urinary Incontinence undergo a suburethral sling operative procedure.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient has objective demonstrable signs of stress urinary incontinence (SUI), including patients with intrinsic sphincter deficiency (ISD). Objective testing includes: standing stress test, urodynamics evaluation, or pad test.

• Patient is age 18 or older.

• Patient agrees to participate in the study, including completion of all study-related procedures and evaluations, and documents this agreement by signing the IRB/EC-approved informed consent.

• Patient is able to fill in all questionnaires (on judgement of investigator)

Locations
Other Locations
Switzerland
Blasenzentrum, Cantonal Hospital
RECRUITING
Frauenfeld
Contact Information
Primary
Volker Viereck, Physican
volker.viereck@stgag.ch
++41 52 723 70 50
Backup
Oliver Rautenberg, Physican
oliver.rautenberg@stgag.ch
++41 52 723 77 45
Time Frame
Start Date: 2013-05
Estimated Completion Date: 2025-07
Participants
Target number of participants: 100
Treatments
Stress Urinary Incontinence
Females with stress urinary incontinence, who undergo a tension free surgical sling procedure.
Sponsors
Leads: Cantonal Hospital, Frauenfeld

This content was sourced from clinicaltrials.gov