Pudendal Block Versus Penian Block For Circumcision In Children

Status Recruiting

Clinical Trial Summary

The authors study the efficacy of the pudendal versus penile block for the relief of postoperative pain in children receiving ambulatory circumcision.

In this prospective, double-blind, randomized, parallel-arm trial, 60 children recruited during the anesthesia consultation will be allocated a general anesthesia with a pudendal block (PUD group) or a penile block (PEN group).

Each block will be made with equal parts lidocaine 1% and ropivacaine 0.75% (0.3 ml/kg).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03046290
Study type	Interventional
Source	Université Libre de Bruxelles
Contact	John Nicolardot, MD
Phone	+3225555288
Email	nicolardotjohn@gmail.com
Status	Recruiting
Phase	N/A
Start date	January 2017
Completion date	April 2017

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