Cohort Study of Bowel Function Following Robotic-assisted Laparoscopic Sacrocolpopexy

Atlantic Health System

Status: Completed

Conditions: Irritable Bowel Syndrome; Pelvic Organ Prolapse; Constipation; Bowel Dysfunction

Treatments: Procedure: Robotic sacral colpopexy

Study type: Observational

Funder types: Other

Identifiers

NCT01618292

R11-08-011

Details and patient eligibility

About

Compare changes in bowel function before, 6 months and one year after Robotic-assisted laparoscopic sacral colpopexy. Compare objective anatomic outcomes before, 6 months and one year after Robotic-assisted laparoscopic sacral colpopexy.

Enrollment: 393 patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion criteria

• All patients who underwent robotic assisted laparoscopic sacral colpopexy

Exclusion criteria

• Any other procedure for the treatment of pelvic organ prolapse

Trial design

393 participants in 1 patient group

Robotic-assisted sacrocolpopexy patients

Description:

Patients who underwent robotic-assisted laparoscopic sacrocolpopexy between January 2007 and August 2011.

Treatment:

Procedure: Robotic sacral colpopexy