One Year Outcome After Robotic Assisted Laparoscopic Sacral Colpopexy, a Case Series Review

Atlantic Health System

Status: Completed

Conditions: Pelvic Organ Prolapse; Urinary Incontinence

Study type: Observational

Funder types: Other

Identifiers

NCT01055860

R09-02-007

Details and patient eligibility

About

Robotic approach to sacral colpopexy is a relatively new procedure. The literature is scarce in regard to its long-term outcomes. This advanced procedure is offered at MMH through the Urogynecology division. The Investigators setup to review the one year outcome of patients who underwent this procedure using a polypropylene mesh. These outcomes will include anatomical and quality of life measures.

Enrollment: 75 estimated patients

Sex: Female

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Any Robotic assisted laparoscopic sacral colpopexy with polypropylene mesh during the study period

Exclusion criteria

• Other graft material than polypropylene.
• Enrollment in a different study.

Trial design

75 participants in 1 patient group

Robotic sacral colpopexy

Description:

Our study population will be women who underwent Robotic assisted laparoscopic sacral colpopexy at the Morristown Memorial Hospital for correction of pelvic organ prolapse using a synthetic polypropylene mesh.