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临床试验/NCT03495388
NCT03495388已完成不适用

Pharmacogenetics and Pharmacokinetics of Oxycodone to Personalize Postoperative Pain Management Following Major Inpatient Surgery in Children

Senthil Sadhasivam2 个研究点 分布在 1 个国家目标入组 129 人开始时间: 2018年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
129
试验地点
2
主要终点
Look at genetic factors predisposing children to immediate postoperative opioid-adverse effects (RD and PONV).

研究概览

简要总结

Each year, in the U.S. alone, >6 million children undergo painful surgery; up to 50% of them experience significant and serious side effects with opioids and inadequate pain relief. Though 60% of this inter-individual variability in responses results from genetic variations, there is an almost complete lack of understanding of how specific genetic variability affects pain and of the adverse effects of opioids, especially in children. In this project the investigators will focus on oxycodone, a standard and preferred post-surgical oral analgesic in children

The purpose of this research is to study serious immediate and long-term clinical problems from both surgical pain and oxycodone use in children and adolescents to improve the safety and effectiveness of surgical pain relief.

The long-term goals are to improve the safety and effectiveness of surgical pain relief with opioids (a class of drugs/pain relievers) and to minimize the societal burden of disabling Chronic Persistent Surgical Pain (CPSP, which is pain that persists even after the expected healing time from surgery) and Opioid Dependence (OD) by preoperative risk predictions and personalized care with the right dose of the right pain medication for each child.

The overall objective is to determine the impact of risk factors on oxycodone's immediate and long-term negative postoperative outcomes and to personalize dosing in children undergoing outpatient and major inpatient surgery.

详细描述

Research procedures will include:

  1. Pre-operative blood draw for genotyping candidate genes and exploratory genes and for future similar studies will be collected.
  2. Standardized pre-, intra-, and post-operative care will be received by all participants. The study team will record medical history, demographic information, concomitant medications, vitals, pain scores, post-operative nausea and vomiting, and all medications given post-surgery for pain management throughout the participants in-patient stay.
  3. Psychological questionnaires to assess pain, risk of developing OD and chronic pain, anxiety and depression will be administered pre-operatively, and 48-72 hours, 7-14 days, 2 months, 3 months, 6 months and 12 months post-operatively.
  4. Quantitative Sensory Testing will be performed on up to 100 participants pre-operatively, and 48-72 hours,3 months and 12 months post-operatively.
  5. Serial blood draws for oxycodone and methadone pharmacokinetic modeling will be collected from up to 200 participants. QTc measurements will also be recorded from pre- and post-operative EKGs for those participants in which methadone pharmacokinetic blood samples are collected.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
8 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Boy and girls
  • All races
  • ASA physical status 1 and 2
  • Scheduled for pectus excavatum repair or idiopathic scoliosis spinal fusion
  • Children with OSA will be included but stratified as they have more opioid-related complications.

排除标准

  • Allergy to oxycodone or methadone
  • Developmental delay
  • Neurological disorder
  • Renal or liver disease
  • Pre-operative pain requiring analgesics
  • On inhibitors or inducers of CYP2D6 and CYP3A
  • Cannot read, write and speak English fluently

研究组 & 干预措施

Major Inpatient Surgeries

Children ages 8-17.9 undergoing pectus excavatum or idiopathic scoliosis spinal fusion at Riley Hospital for Children, who have consented to participate in an observational clinical study as approved by the IU IRB, protocol #1707525204.

干预措施: Oxycodone (Drug)

结局指标

主要结局

Look at genetic factors predisposing children to immediate postoperative opioid-adverse effects (RD and PONV).

时间窗: Immediately post-surgery during hospital stay and at home up to 1 year post-surgery

The investigators will look at specific CYP2D6, ABCB1, FAAH, OPRM1, and COMT variants to find correlations with children who experience RD, and PONV in the immediate post-surgical period (4 days) in the hospital and at home.

Look at genetic factors predisposing children to inadequate surgical pain relief with oxycodone.

时间窗: Immediately post-surgery during hospital stay and at home up to 1 year post-surgery

The investigators will look at specific CYP2D6, ABCB1, FAAH, OPRM1, and COMT variants to find correlations with children who experience poor pain relief in the immediate post-surgical period (4 days) in the hospital and at home.

次要结局

  • Look at the impact of CYP2D6 variants on oxycodone's clinical dosing in children to see if specific variants correlate with a need for lower or higher doses of analgesic.(Pre-operative to post-operative day 2)

研究者

发起方
Senthil Sadhasivam
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Senthil Sadhasivam

Professor

University of Pittsburgh

研究点 (2)

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