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临床试验/NCT01988922
NCT01988922已完成不适用

Role of CYP2B6 Polymorphisms in Ketamine Metabolism and Clearance

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2013年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
1
主要终点
The Effects of CYP2B6 Genetic Variants on Ketamine Metabolism and Clearance by CYP2B6*6 Hetero or Homozygote Genotype.

研究概览

简要总结

This research study will determine if genetic variation in CYP2B6 affects how the body metabolizes ketamine.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 18-50 yr old
  • CYP2B6*1/*1, CYP2B6*1/*6 or CYP2B6*6/*6 genotype (see table) (Note: subjects of other rare genotype but with one or more 516G>T, 785A>G, 983T>C or 1459C>T polymorphism may be enrolled at PI's discretion)
  • Good general health with no remarkable medical conditions
  • Provided informed consent

排除标准

  • Known history of liver or kidney disease
  • Use of prescription or non prescription medications, herbals, foods or chemicals known to be metabolized by or affecting CYP2B6
  • Females who are pregnant or nursing
  • Known history of drug or alcohol addiction (prior or present addiction or treatment for addiction)
  • Direct physical access to and routine handling of addicting drugs in the regular course of duty (this is a routine exclusion from studies of drugs with addiction potential)

研究组 & 干预措施

Ketamine arm- *1/*1

Experimental

1.*1/*1- oral racemic ketamine 0.4 mg/kg

干预措施: ketamine (Drug)

Ketamine arm - *1/*6

Experimental
  1. *1/*6- oral racemic ketamine 0.4 mg/kg

干预措施: ketamine (Drug)

Ketamine arm - *6/*6

Experimental
  1. *6/*6- oral racemic ketamine 0.4 mg/kg

干预措施: ketamine (Drug)

结局指标

主要结局

The Effects of CYP2B6 Genetic Variants on Ketamine Metabolism and Clearance by CYP2B6*6 Hetero or Homozygote Genotype.

时间窗: up to 24 hours

Ketamine metabolism, measured as the plasma norketamine/ketamine AUC ratio in CYP2B6\*6 carriers (CYP2B6\*6 hetero or homozygotes) compared to the wild-type CYP2B6\*1/\*1 genotype Ketamine, norketamine, and dehydronorketamine concentrations in plasma and urine were determined by enantioselective HPLC tandem mass spectrometry, using solid phase extraction, based on a modification of a published method.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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CYP2B6 Polymorphisms in Ketamine | 临床试验