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Clinical Trial Summary

This study evaluates post-operative pain between different insufflation pressures during robotic-assisted sacrocolpopexy. Subjective pain and narcotic usage after surgery will be measured.


Clinical Trial Description

This is a prospective single-blind randomized controlled trial of adult women undergoing robotic-assisted sacrocolpopexy for pelvic organ prolapse. Each surgery will be performed by a board-certified Female Pelvic Medicine & Reconstructive Surgery (FPMRS) surgeon with a standard technique other than pneumoperitoneum level. A sacrocolpopexy for apical prolapse may be performed at the same time as a hysterectomy and other clinically indicated procedures if desired by the patient and as part of the standard of care. Patients will be stratified by hysterectomy prior to randomization. Postoperatively, patients will be evaluated with a Visual Analogue Scale (VAS) as well as prescribed narcotic analgesic use and followed up to 2 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04858438
Study type Interventional
Source Ascension South East Michigan
Contact Gabriella Rustia, MD
Phone 313-343-6708
Email [email protected]
Status Recruiting
Phase N/A
Start date April 2, 2021
Completion date December 31, 2022

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