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Clinical Trial Summary

Proctological surgery represents a short duration surgery performed in ambulatory, which causes significant post-operative pain.

Post-operative pain resulting from proctological surgery is greater than 5 on the Visual Analog Scale (VAS) within the first 24 hours and it revives during the first defecation.

The ideal pain management procedures are based on the multimodal analgesia model, based in turn on the combination of products and / or techniques to improve the quality of analgesia, reduce the side effects linked to the use of opioids, reduce responses to surgical stress, reduce postoperative recovery and allow rapid rehabilitation of the patient.

The aim of our study is to investigate whether clonidine combined with levobupivacaine in the pudendal block reduce the total consumption of opioids in proctological surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04530903
Study type Interventional
Source Centre Hospitalier Universitaire Saint Pierre
Contact Panayota Kapessidou, MD,PhD
Phone +32.2.535
Email pkapessi@ulb.ac.be
Status Recruiting
Phase Phase 4
Start date September 9, 2020
Completion date January 1, 2021