Overview
This study aims to confirm the perioperative and early postoperative safety and clinical performance (efficacy) of the Dexter Robotic System, in patients undergoing robotic-assisted sacrocolpopexy or sacrocervicopexy.
Eligibility
Inclusion Criteria:
- Aged > 18 years
- Women with symptomatic stage I or greater pelvic organ prolapse (POP-Q)
- Patient agrees to perform the 6-week follow-up assessment as per Standard of Care
Exclusion Criteria:
- Any planned non-urogynaecological concomitant procedures
- History of previous POP surgery, with the exception of transvaginal approaches without mesh implantation
- Previous surgery and/or radiation for urologic, gastrointestinal or gynecologic cancer
- History of Crohn's disease
- Chronic colitis