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Analgesic Efficiency of Pudendal Nerve Block Versus Penil Block for Circumsion in Children

Postoperative Analgesia Clinical Trial

Official title:
Comparison of Analgesic Efficiency of Pudendal Nerve Block and Penil Block for Circumsion in Children

Clinical Trial Summary

The aim of this prospective randomized study is to assess the analgesic efficacy of Pudendal block compared with penil block for pediatric patients undergoing circumsion concerning postoperative analgesic consumption within 24 hours.

Clinical Trial Description

In this prospective study, patients will be randomized into 2 groups, either receiving penil Block( PNL) or nerve stimulator-guided Pudendal Nerve Block(PNB). Analgesic consumption will be assessed during the first 24 hours postoperatively. The "CHEOPS pain scale" will use to assess postoperative pain. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03258255
Study type Interventional
Source Istanbul University
Contact
Status Completed
Phase N/A
Start date November 2016
Completion date July 2017
View Details
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