CompletedNot Applicable

Surgical Management for Suburethral Slings

Switzerland100 participantsStarted 2013-05

Plain-language 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.

Who can participate

Age range18 Years

SexFEMALE

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Inclusion criteria

✓. 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)

Exclusion criteria

✕. Patient has an associated or suspected neurological disease.
✕. Patient has an active lesion or present injury to perineum or urethra.
✕. Patient has a urethral obstruction.
✕. Patient has significant pelvic organ prolapse (Grade III/IV) requiring surgical treatment.
✕. The subject has current urinary tract infection.

What they're measuring

Cure/improvement rate

Timeframe: 3 months

Trial details

NCT IDNCT02785016

SponsorCantonal Hospital, Frauenfeld

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-12

View on ClinicalTrials.gov More Stress Urinary Incontinence trials