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Bilateral Erector Spinae Plane Block as an Opioid Sparing Technique for Selective Dorsal Rhizotomy in Pediatric Patients With Spastic Cerebral Palsy

T

Tanta University

Status

Completed

Conditions

Sparing
Erector Spinae Plane Block
Spastic Cerebral Palsy
Selective Dorsal Rhizotomy
Pediatric
Opioid

Treatments

Other: Erector Spinae Plane Block

Study type

Interventional

Funder types

Other

Identifiers

NCT06600061
36264PR838/9/24

Details and patient eligibility

About

This study aims to evaluate the efficacy of bilateral erector spinae plane block as an opioid-sparing technique for selective dorsal rhizotomy in pediatric patients with spastic cerebral palsy.

Full description

Cerebral palsy (CP) is the most common physical disability affecting children. Selective dorsal rhizotomy (SDR) is a neurosurgical procedure that permanently reduces lower limb spasticity in children with CP by selectively targeting and removing sensory rootlets with aberrant activity.

Postoperative pain is often distressing for patients and their families and can result in complications, delayed participation in therapy, and poor functional recovery. Erector spinae plane block (ESPB) is a newly described interfascial plane block. ESPB is effective on both visceral and somatic pain.

Enrollment

30 patients

Sex

All

Ages

6 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age from 6 to 18 years.
  • Both sexes.
  • American Society of Anesthesiology (ASA) physical status II, III.
  • Patients with spastic cerebral palsy undergoing selective dorsal rhizotomy.

Exclusion criteria

  • Allergy to local anesthetics.
  • Severe fixed joint deformity.
  • Previous orthopedic surgery.
  • Patient with abnormal liver/kidney function.
  • Patient with skin damage or infection at the proposed puncture site.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Erector Spinae Plane Block group
Experimental group
Description:
Patients will receive erector spinae plane block after induction of anesthesia.
Treatment:
Other: Erector Spinae Plane Block
Control group
No Intervention group
Description:
Patients will not receive erector spinae plane block.

Trial contacts and locations

1

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Central trial contact

Mohammed S Elsharkawy, MD

Data sourced from clinicaltrials.gov

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