NCT04586166View on ClinicalTrials.gov

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

NARecruitingINTERVENTIONAL
Enrollment

180

Participants

Timeline

Start Date

December 23, 2020

Primary Completion Date

December 31, 2031

Study Completion Date

December 31, 2032

Conditions
Stress Urinary IncontinencePelvic Floor Disorders
Interventions
DEVICE

RP Sling

Participants assigned to the retropubic (RP) sling group will have the RP sling placement procedure.

DEVICE

SIS

Participants assigned to the single-incision sling (SIS) group will have the SIS placement procedure.

Trial Locations (7)

8001

SUSPENDED

Pelvic Floor Foundation of South Africa, University of Cape Town, Cape Town

27101

RECRUITING

Wake Forest Baptist Medical Center, Winston-Salem

30912

RECRUITING

Augusta University, Augusta

33073

ACTIVE_NOT_RECRUITING

Florida Robotic and Minimally Invasive Urogynecology, Coconut Creek

60611

ACTIVE_NOT_RECRUITING

Northwestern Medicine, Chicago

60637

RECRUITING

University of Chicago, Chicago

02138

RECRUITING

Boston Urogynecology Associates, Cambridge

Sponsors
All Listed Sponsors
collaborator

Boston Scientific Corporation

INDUSTRY

lead

Wake Forest University Health Sciences

OTHER

NCT04586166 - Single-incision Versus Retropubic Mid-Urethral Sling (Solyx) for SUI During Minimally Invasive Sacrocolpopexy | Biotech Hunter | Biotech Hunter