Laparoscopic Versus Robotic Assisted Laparoscopic Sacrocolpopexy for Vaginal Prolapse

Completed · Not applicable

Conditions studied: Pelvic Organ Prolapse

In brief

The purpose of this study is to conduct a trial of robotic assisted versus traditional laparoscopic sacrocolpopexy in the treatment of patients with vaginal prolapse.

Key facts

Study ID

NCT00551993

Run by

The Cleveland Clinic

People needed

78

Starts

2006-09-01

Expected to finish

2011-11-01

Last updated by the study team

2014-02-19

Who can join

Age: 21 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women who are 21 years of age or greater
• Status post hysterectomy with apical vaginal prolapse POPQ stages II-IV (prolapse from 1cm proximal to the hymen to all points distal) that desire laparoscopic surgical management.

You may not qualify if…

• Patients that are not candidates for general anesthesia
• Inability to consent
• History of prior sacralcolpopexy
• Suspicious adnexal masses or other factors that may indicate pelvic malignancy
• History of pelvic inflammatory disease
• Morbid obesity (body mass index greater than or equal to 40)
• History of prior or need for concomitant rectopexy with sigmoid resection.

Where it is running

• Cleveland Clinic — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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