Postoperative Analgesia
Conditions
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.
Interventions
PROCEDUREpenil or pudendal nerve block in circumcision
regional analgesia methods during the circumsion nerve stimulator guided pudendal block performed by anesthesiologist/ penil block performed by surgeon before circumcision
Sponsors
Istanbul University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)
Eligibility
Sex/Gender
MALE
Age
1 Years to 12 Years
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Postoperative pain evaluatiom | 24 hour | CHEOPS pain scale |
Outcome results
None listed