Perianal Nerval Block in Proctological Interventions

Status Completed

Clinical Trial Summary

The aim of this study is to evaluate whether a local perianal block performed during a proctological intervention can reduce the postoperative pain.

Clinical Trial Description

The aim of this study is to evaluate whether a local perianal block performed during a proctological intervention can reduce the postoperative pain.

All patients will undergo surgery under general or spinal anesthesia. At the end of the surgery, the surgeon will perform a perianal block using the local anesthetic or the placebo upon randomisation. The experimental group will receive a local anesthetics and the control group a normal saline injection. All injections will be perianal, peripheral to the external anal sphincter. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03405922
Study type	Interventional
Source	University Hospital, Basel, Switzerland
Contact
Status	Completed
Phase	Phase 4
Start date	February 1, 2018
Completion date	July 5, 2019

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