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Caudal Epidural Block Versus Ultrasound-Guided Pudendal Nerve Block for Pediatric Circumcision

P

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Status

Completed

Conditions

Circumcision

Treatments

Procedure: Pudendal nerve block group
Procedure: Caudal epidural block group

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The regional anesthesia methods of caudal epidural block (CEB) and dorsal penile nerve block (DPNB) play an important role in providing postoperative pain control in pediatric circumcision surgery. However, the short-term postoperative analgesic effect and the risk of block failure limit the use of DPNB, a peripheral nerve block.

Full description

CEB is a neuraxial block and commonly used to control moderate and severe postoperative pain following surgery related to the lumbosacral and midthoracic dermatomes. CEB can have serious undesirable complications such as intravascular and subarachnoid injection, urinary retention and motor block. Pudendal nerve block can be used as an alternative to both DPNB and CEB for penile surgery such as circumcision. The pudendal nerve is a peripheral nerve combining the anterior rami of the sacral plexus nerves (S2-S4) and provides motor and sensory innervation to the perineal region.

Enrollment

100 patients

Sex

All

Ages

4 to 12 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male patients aged between 4-12 years
  • ASA (American Society of Anesthesiologists) I-II group
  • Scheduled for circumcision
  • Able to communicate in Turkish
  • Willing to participate to the study (parents and children)

Exclusion criteria

  • Patients aged less than 4 or more than 12 years
  • Neurological deficit
  • Bleeding diathesis
  • History of local anesthetic allergy
  • Current infection or redness in the region to be injected
  • Congenital lower back anomaly
  • Liver disease
  • Psychiatric disorder
  • Mental retardation
  • Communication problem
  • Refusal to participate in the study.

Trial design

100 participants in 2 patient groups

Caudal epidural block group
Description:
Linear ultrasound probe and the sacral hiatus at the sacral cornu level was visualized using an out-of-plane transverse view at 5-10 megahertz . The linear probe was then rotated 90 degrees and placed longitudinally in the midline to evaluate the sacral cornus, sacrococcygeal ligament and sacral bone.
Treatment:
Procedure: Caudal epidural block group
Pudendal nerve block group
Description:
The long axis of the ultrasound probe was positioned on a horizontal line connecting the ischial tuberosity that had been previously located by palpation to the anus. The ischial tuberosity could be easily identified as a hypoechoic area that is bounded superiorly by a hyperechoic line. The probe was then moved medially on the same axis until the rectum appeared as another hypoechoic area.
Treatment:
Procedure: Pudendal nerve block group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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