NCT06935331
Prospective Opioid-Free AIS Fusion
Enrolling by Invitation
PHASE4Ages 10–20InterventionalTreatmentOrthoCarolina Research Institute, Inc.Investigator-initiated
~58 participants
Updated 2026-04-06 on ClinicalTrials.gov
What's tested:Opioid-Free/Opioid-AvoidantOpioid-Containing
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Pain rating on the 10-point numeric pain rating scale (NPRS)
Measured over 24 hours after surgery completion
Conditions
Where it's being run
1 sites across 1 statesNorth Carolina1
Study leadership
- Michael Paloski, DO · PRINCIPAL_INVESTIGATOR · OrthoCarolina Research Institute, Inc.
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Pediatric patients (10-20 years of age at the time of surgery)
Diagnosis of idiopathic scoliosis
Undergoing primary instrumented PSF
Exclusion
Age \<10 years or \>20 years at time of surgery
Patients with non-idiopathic scoliosis etiology, ie neuromuscular or syndromic scoliosis
Patients undergoing non-fusion spinal surgeries, ie growing rods or tethering
What this trial measures
- Pain rating on the 10-point numeric pain rating scale (NPRS)24 hours after surgery completion
Pain rating on the 10-point numeric pain rating scale (NPRS) 24 hours after surgery completion