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

Istanbul University80 enrolled

Overview

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.

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 Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Postoperative Analgesia

Interventions

penil or pudendal nerve block in circumcisionPROCEDURE

regional analgesia methods during the circumsion nerve stimulator guided pudendal block performed by anesthesiologist/ penil block performed by surgeon before circumcision

Eligibility

Sex: MALEMin age: 1 YearMax age: 12 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Outcomes

Primary Outcomes

Postoperative pain evaluatiom

CHEOPS pain scale

Time frame: 24 hour

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.