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Propofol + Remifentanil vs. Propofol + Dexmedetomidine in Adolescent Idiopathic Scoliosis Patients Having Spine Surgery

Primary Purpose

Adolescent Idiopathic Scoliosis, Multimodal Analgesia, Opioid Induced Hyperalgesia

Status
Not yet recruiting
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Remifentanil TIVA
Dexmedetomidine TIVA
Propofol TIVA
Sponsored by
Cedars-Sinai Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Adolescent Idiopathic Scoliosis

Eligibility Criteria

12 Years - 18 Years (Child, Adult)All SexesAccepts Healthy Volunteers

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

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Propofol + Remifentanil

    Propofol + Dexmedetomidine

    Arm Description

    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.

    Outcomes

    Primary Outcome Measures

    Total opioid consumption (IV and PO in MME) on POD# 0 and 1
    Measure the total opioid medications needed by the participant (IV and oral) after surgery on post operative days # 0 and 1.

    Secondary Outcome Measures

    Average VAS Pain score on POD# 0 and 1
    Measure the average pain score of the participant on a visual analog pain scale. The VAS has two end points representing 0 ("no pain") and 10 ("worst pain ever"). It is reported at our institution as a number between 0 and 10.
    Time from skin closure to participant being able to move their feet on command (mins)
    Measure the time (mins) from completion of surgical skin closure to the participant being able to move their feet to command
    Time from skin closure to Extubation
    Measure the time (mins) from completion of surgical skin closure to extubation

    Full Information

    First Posted
    October 16, 2023
    Last Updated
    October 19, 2023
    Sponsor
    Cedars-Sinai Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06096181
    Brief Title
    Propofol + Remifentanil vs. Propofol + Dexmedetomidine in Adolescent Idiopathic Scoliosis Patients Having Spine Surgery
    Official Title
    A Prospective Study Comparing Total Intravenous Anesthesia With Propofol and Remifentanil vs. Propofol and Dexmedetomidine in Adolescent Idiopathic Scoliosis Patients Undergoing Posterior Spinal Fusion and Instrumentation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 2023 (Anticipated)
    Primary Completion Date
    December 2027 (Anticipated)
    Study Completion Date
    June 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Cedars-Sinai Medical Center

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    Yes

    5. Study Description

    Brief Summary
    Patients with Adolescent Idiopathic Scoliosis may need surgery to correct their scoliosis. General anesthesia is required for this surgery, and a multimodal analgesic regimen using combinations of opioid and non-opioid medications is the standard of care. The purpose of this study is to compare two combinations of total intravenous anesthetic medications in children with Adolescent Idiopathic Scoliosis having posterior spinal fusion surgery. Participants in the study will be randomly selected to receive either Propofol and Remifentanil or Propofol and Dexmedetomidine as their total intravenous anesthesia (TIVA). TIVA is favored over gas anesthesia because gas anesthesia can affect the neurological monitoring necessary for this surgery. The first combination (Propofol + Remifentanil) is the most common one used for this surgery at our institution, and the second combination (Propofol + Dexmedetomidine) is more commonly used in adult spine surgery. Though Dexmedetomidine is not approved for pediatric use by the FDA, it is widely used in pediatric patients for procedural sedation and surgical anesthesia in the US and worldwide. Both anesthetic combinations are used safely in adult and pediatric patients at our institution. Although remifentanil works fast and is an excellent pain medication during surgery, there are reports that it's use can cause increased pain sensitivity and greater need for narcotic pain medication after surgery. This phenomenon is known as opioid-induced hyperalgesia. The investigators hypothesize that avoiding the use of remifentanil in the TIVA by using dexmedetomidine could avoid OIH and thus result in superior postop pain control. Our study's primary goal is to measure the total opioid consumption on postoperative days (POD)# 0 and 1. Our secondary goals are to measure the pain scores on a visual analog scale (VAS) on POD# 0 and 1, measure the time it takes for participants to move their feet to command when surgery is done, and measure the time it takes for participants to be extubated when surgery is done. By comparing these measurements, the investigators hope to find out if there is any significant difference between the two TIVAs in terms of postop opioid requirements, pain scores, and time to wake up from anesthesia. The investigators hope that our study gives us more knowledge on how to better treat postoperative pain in children who have spine surgery to correct their
    Detailed Description
    Patients with Adolescent Idiopathic Scoliosis (AIS) may need surgery to correct their scoliosis. General anesthesia is required for this surgery, and a multimodal analgesic regimen using combinations of opioid and non-opioid medications is the standard of care. Total intravenous anesthesia (TIVA) is the usual anesthetic technique of choice. The purpose of this study is to compare two combinations of TIVA medications in children AIS having posterior spinal fusion surgery. The most common TIVA for this surgery at our institution is Propofol + Remifentanil. Remifentanil is a popular choice because of its rapid onset, extremely short context-sensitive half-life, potency, and its rapid recovery from drug effect. However, an important concern with intraoperative remifentanil infusion is the possible development of acute opioid-induced hyperalgesia (OIH). In adults, OIH is a well-documented feature linked to intraoperative remifentanil administration, manifesting as increased postoperative analgesic requirement and paradoxical increase in sensitivity to painful stimuli. In pediatric patients, the phenomenon is not as well characterized. An alternative TIVA that is very commonly used for adult spine surgery is propofol + dexmedetomidine (DEX). DEX is a highly selective alpha2-adrenergic receptor agonist with sedative, analgesic, and sympatholytic properties. Despite the lack of FDA approval for pediatric use, DEX is widely used off-label in pediatric patients in the US and worldwide and has previously been shown to be safe and efficacious for various clinical indications including procedural sedation, craniotomy-awake-surgery, cardiac surgery, and posterior spinal fusion for scoliosis. DEX is currently used safely in pediatric and adult spine patients in our institution. The most common adverse effect is intraoperative bradycardia. Participants will be randomized to receive one of the two TIVAs to see if one or the other results in lower opioid consumption, and lower Visual Analog Scale (VAS) pain scores in the post-operative period (POD# 0 and 1). The investigators hypothesize that the use of DEX will avoid OIH and this will lead to less opioid consumption in the postoperative period, and superior postoperative pain control. The investigators also hope to show that the use of DEX will not significantly prolong time to moving feet to command and extubation at conclusion of surgery.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Adolescent Idiopathic Scoliosis, Multimodal Analgesia, Opioid Induced Hyperalgesia, Remifentanil, Dexmedetomidine, Posterior Spinal Fusion

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare Provider
    Masking Description
    The following persons are masked: Participant and parents Pediatric Intensive Care Unit (PICU) staff taking care of patient postoperatively Surgeon
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Propofol + Remifentanil
    Arm Type
    Active Comparator
    Arm Description
    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.
    Arm Title
    Propofol + Dexmedetomidine
    Arm Type
    Active Comparator
    Arm Description
    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.
    Intervention Type
    Drug
    Intervention Name(s)
    Remifentanil TIVA
    Other Intervention Name(s)
    Ultiva TIVA
    Intervention Description
    Remifentanil is more commonly used in the TIVA combination for pediatric patients having this surgery.
    Intervention Type
    Drug
    Intervention Name(s)
    Dexmedetomidine TIVA
    Other Intervention Name(s)
    Precedex TIVA
    Intervention Description
    Dexmedetomidine is less commonly used in the TIVA combination for pediatric patients having this surgery.
    Intervention Type
    Drug
    Intervention Name(s)
    Propofol TIVA
    Other Intervention Name(s)
    Diprivan TIVA
    Intervention Description
    Propofol is an anesthetic drug that causes sleep during surgery.
    Primary Outcome Measure Information:
    Title
    Total opioid consumption (IV and PO in MME) on POD# 0 and 1
    Description
    Measure the total opioid medications needed by the participant (IV and oral) after surgery on post operative days # 0 and 1.
    Time Frame
    Post Op Day# 0 and 1
    Secondary Outcome Measure Information:
    Title
    Average VAS Pain score on POD# 0 and 1
    Description
    Measure the average pain score of the participant on a visual analog pain scale. The VAS has two end points representing 0 ("no pain") and 10 ("worst pain ever"). It is reported at our institution as a number between 0 and 10.
    Time Frame
    Post Op Day# 0 and 1
    Title
    Time from skin closure to participant being able to move their feet on command (mins)
    Description
    Measure the time (mins) from completion of surgical skin closure to the participant being able to move their feet to command
    Time Frame
    Intraoperative (day of surgery)
    Title
    Time from skin closure to Extubation
    Description
    Measure the time (mins) from completion of surgical skin closure to extubation
    Time Frame
    Intraoperative (day of surgery)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    12 Years
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    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
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Glenn Tan
    Phone
    3104235841
    Email
    glenn.tan@cshs.org
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Glenn Tan, M.D.
    Organizational Affiliation
    Cedars-Sinai Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    Propofol + Remifentanil vs. Propofol + Dexmedetomidine in Adolescent Idiopathic Scoliosis Patients Having Spine Surgery

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