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Clinical Trial Summary

The objective of this this randomized controlled study is to determine whether a pudendal nerve block at the time of vaginal surgery is associated with improved postoperative pain control and decrease opioid consumption compared to a sham pudendal nerve block in patients undergoing vaginal surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04198714
Study type Interventional
Source MetroHealth Medical Center
Contact
Status Active, not recruiting
Phase N/A
Start date August 1, 2019
Completion date June 30, 2022

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