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Single-incision Versus Retropubic Mid-Urethral Sling (Solyx) for SUI During Minimally Invasive Sacrocolpopexy — SASS  

Stress Urinary Incontinence Clinical Trial

Official title:
SASS: Randomized Trial of Single-incision Versus Retropubic Mid-Urethral Sling (Solyx) for Concomitant Management of Stress Urinary Incontinence During Minimally Invasive Sacrocolpopexy

Clinical Trial Summary

SASS (Single-incision Versus Retropubic Mid-Urethral Sling (Solyx) for SUI During Minimally Invasive Sacrocolpopexy) will be a multicenter, prospective, randomized, single-blind non-inferiority trial.

Clinical Trial Description

SASS aims to compare the efficacy of a single-incision (SIS) versus a retropubic mid-urethral sling (RP) placed at the time of minimally invasive sacrocolpopexy in women with pelvic organ prolapse and objectively confirmed stress urinary incontinence (SUI). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04586166
Study type Interventional
Source Wake Forest University Health Sciences
Contact Sachin N Vyas, MS,PhD
Phone 336-713-4098
Email svyas@wakehealth.edu
Status Recruiting
Phase N/A
Start date December 23, 2020
Completion date December 2032
View Details
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