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Clinical Trial Summary

Primary purpose: Show the pain improvement 3-month after robotic laparoscopic pudendal nerve decompression for pudendal neuralgia. Primary outcomes: Pain evaluated on a VAS before surgery and 3-month after surgery or surveillance Improvement is considered if pain decreased by at least 3/10 points on the VAS. Secondary purposes: - improvement of quality of life - study of MRI performance to predict pudendal nerve entrapment topography - show the feasibility and safety of robotic pudendal nerve decompression


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03876977
Study type Interventional
Source University Hospital, Strasbourg, France
Contact
Status Terminated
Phase N/A
Start date August 8, 2020
Completion date September 23, 2021