Erector Spinae Plane Blockade in Pediatric Scoliosis Surgery Patients

Recruiting N/A Interventional Study
Scoliosis; Juvenile Scoliosis; Adolescence
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
Up to 18
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
50 (estimated)
Sponsor
Stanford University · Other
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About This Trial
Providing effective analgesia after spinal fusion for idiopathic scoliosis remains a challenge with significant practice variation existing among high volume spine surgery centers. Even in the era of multimodal analgesia, opioids are the primary analgesics used for pain control after pediatric scoliosis surgery, but have multiple known adverse effects. The erector spinae plane block (ESPB) is a ne…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * ASA I-III * Diagnosed with Idiopathic scoliosis * Undergoing single-stage posterior spinal instrumentation and fusion Exclusion Criteria: * Thorascopic tethering procedure * Two-stage procedure * Abnormal developmental profile * Congenital/neuromuscular scoliosis * Requiring…
Contacts

Ban Tsui, MD

(650)200-9107

bantsui@stanford.edu

CONTACT

Chynna Villanueva, BS, RN

6504986346

chynnav@stanford.edu

CONTACT