Single Incision Suburethral Sling at Time of Robotic Sacrocolpopexy

Atlantic Health System

Status: Completed

Conditions: Stress Urinary Incontinence (SUI)

Study type: Observational

Funder types: Other

Identifiers

NCT01982188

R12-09-001

Details and patient eligibility

About

This study was designed to evaluate urinary function before and one year after single incision sling placement at the time of robotic sacrocolpopexy. The thought is that the more minimally-invasive, single incision sling would provide a similar subjective success rates as those of retropubic and trans-obturator slings.

Enrollment: 104 patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion criteria

• all patients undergoing single incision sling placement at the time of robotic sacrocolpopexy during the study period

Exclusion criteria

• previous surgical treatment for stress urinary incontinence (SUI)

Trial design

104 participants in 1 patient group

Single incision sling