penil or pudendal nerve block in circumcision
Procedureregional analgesia methods during the circumsion nerve stimulator guided pudendal block performed by anesthesiologist/ penil block performed by surgeon before circumcision
NCT Number: NCT03258255
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.
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Notify Me1 year–12 year
Male
Interventional
Not applicable
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
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
regional analgesia methods during the circumsion nerve stimulator guided pudendal block performed by anesthesiologist/ penil block performed by surgeon before circumcision
Time frame: 24 hour
CHEOPS pain scale
Istanbul University
Other
Comparison of Analgesic Efficiency of Pudendal Nerve Block and Penil Block for Circumsion in Children
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