跳至主要内容
临床试验/NCT03087383
NCT03087383Unknown不适用

Identification of Genetic Polymorphisms Related to Propofol Requirement and Recovery Through Genome-wide Association Study (GWAS) in Total Intravenous Anesthesia for Clipping of Unruptured Cerebral Aneurysm in Korean Population

Yonsei University1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2017年3月2日最近更新:
适应症

试验速览

阶段
不适用
入组人数
500
试验地点
1
主要终点
Time of eye opening after stopping propofol infusion

研究概览

简要总结

In neurosurgical anesthesia, propofol based total intravenous anesthesia (TIVA) is frequently used due to brain relaxation and less effect on electrophysiologic monitoring. Response to propofol can vary between individuals and be associated with clinical factors including age and weight, and genetic polymorphism. Because the importance of rapid recovery in neurosurgery with long operation time is emphasized recently, the choice and dose adjustment of anesthetics should be determined according to clinical and genetic factors. Recently, researches about genetic variations have been performed with single nucleotide polymorphism (SNP). The aim of this study is to find SNPs associated with propofol recovery and response through genome-wide association study (GWAS) in Korean adult population undergoing propofol based TIVA for clipping of unruptured cerebral aneurysm.

研究设计

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

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Korean adult population undergoing propofol based TIVA for clipping of unruptured cerebral aneurysm

排除标准

  • Patients not able to read, or understand the consent form
  • Ethnicity, other than Korean population
  • Patients refusal
  • Patients not to perform total intravenous anesthesia
  • Patients currently taking psychiatric medication

结局指标

主要结局

Time of eye opening after stopping propofol infusion

时间窗: Within one hour

When operation is finished, investigator will stop the intravenous infusion of propofol. Investigators will measure the time from when propofol infusion is stopped until eye opening and extubation, respectively. The measurement will be established within about one hour from end of surgery.

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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