Analgesic Efficiency of Pudendal Nerve Block Versus Penil Block for Circumsion in Children
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 80
ASA I-II patients, aged 1-12 years old patient undergoing circumcision,
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
- Secondary Outcome Measures
Name Time Method