The Effect of Erector Spinae Plane Block (ESPB) on Pediatric Pain Management Following Posterior Spinal Fusion (PSF) Surgery

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age10-18
SponsorUniversity of California, San Francisco

About this trial

This study is being done to better understand the efficacy of an erector spinae plane block (ESPB) in pain management for children with Adolescent Idiopathic Scoliosis or Neuromuscular Scoliosis undergoing Posterior Spinal Fusion surgery. The study team is trying to find out if receiving the ESPB leads to less pain and less need for pain medication after surgery.

The ESPB involves an injection of a local anesthetic, ropivacaine, into your child's back muscles to help block pain signals.

Eligibility criteria

Qualifiers

Diagnosis of Adolescent Idiopathic Scoliosis (AIS) or neuromuscular scoliosis

Undergoing Posterior Spinal Fusion (PSF) Surgery

Disqualifiers

Patients with forms of scoliosis other than AIS or NM Scoliosis.

Patients undergoing a spinal deformity correction surgery other than Posterior Spinal Fusion Surgery

Allergy or other contraindication to erector spinae plane block (ESPB) with Ropivacaine patients who are taking pre-operative opioids

Trial design

Treatments tested in this trial

  • Ropivacaine Hydrocloride

Treatment groups

42 Participants
are divided into 2 treatment groups