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

Not Applicable

Completed

• Conditions: Postoperative Analgesia

• Registration Number: NCT03258255
• Lead Sponsor: Istanbul University

Brief 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.

Detailed 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 Timeline

• Study Start: 2016-11
• Primary Completion: 2017-06
• Study Completion: 2017-07
• Study First Submitted: 2017-08-20
• Study First Submitted QC: 2017-08-22
• Study First Posted: 2017-08-23
• Status Verified: 2017-11
• Last Update Submitted: 2017-11-15
• Last Update Posted: 2017-11-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 80

Inclusion Criteria

ASA I-II patients, aged 1-12 years old patient undergoing circumcision,

Exclusion Criteria

history of local anesthetics's allergy, infection at the injection side, anatomical abnormalities, coagulopaty, bleeding disease, liver disease

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Postoperative pain evaluatiom	24 hour	CHEOPS pain scale