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

Istanbul University

Status: Completed

Conditions: Postoperative Analgesia

Treatments: Procedure: penil or pudendal nerve block in circumcision

Study type: Interventional

Funder types: Other

Identifiers

NCT03258255

242893

Details and patient eligibility

About

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.

Full 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.

Enrollment: 80 patients

Sex: Male

Ages: 1 to 12 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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80 participants in 2 patient groups

Pudendal block group in circumcision

Active Comparator group

Description:

Nerve stimulated pudendal nerve block performed under general anesthesia

Treatment:

Procedure: penil or pudendal nerve block in circumcision

Penil block group in circumcision

Active Comparator group

Description:

Penil block performed by surgeon under general anesthesia

Treatment:

Procedure: penil or pudendal nerve block in circumcision