Propofol + Remifentanil vs. Propofol + Dexmedetomidine in Adolescent Idiopathic Scoliosis Patients Having Spine Surgery
Adolescent Idiopathic Scoliosis, Multimodal Analgesia, Opioid Induced Hyperalgesia
About this trial
This is an interventional prevention trial for Adolescent Idiopathic Scoliosis
Eligibility Criteria
Inclusion Criteria: Age 12-18 years old American Society of Anesthesiology Physical Status Classification (ASA Class) 1 and 2 Have diagnosis of Adolescent Idiopathic Scoliosis Undergoing Posterior Spinal Fusion with instrumentation for scoliosis correction Matched on age, sex, and the number of vertebral levels fused Exclusion Criteria: Neuromuscular scoliosis Allergy to any of the multi-modal analgesia regimen drugs Use of serotonergic drugs, monoamine oxidase inhibitors (MAOI), mixed agonist/antagonist opioid analgesics
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Propofol + Remifentanil
Propofol + Dexmedetomidine
Participants are randomly selected to receive Propofol + Remifentanil TIVA as their anesthesia. Dose of IV Propofol is 100-200 mcg/kg/min and dose of Remifentanil is 0.2-0.5 mcg/kg/min. TIVA is titrated to keep bispectral index (BIS) < 55-60 to ensure patient is asleep.
Participants are randomly selected to receive Propofol + Dexmedetomidine as their anesthesia. Dose of Propofol is 100-200 mcg/kg/min and dose Dexmedetomidine is ) 0.2-0.7 mcg/kg/hr. TIVA is titrated to beep bispectral index (BIS) < 55-60 to ensure patient is asleep.