跳至主要内容
临床试验/NCT00731900
NCT00731900Unknown不适用

Pharmacogenetic Study for Topiramate-Induced Cognitive Dysfunction

National Taiwan University Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2007年4月最近更新:
适应症

试验速览

阶段
不适用
入组人数
100
试验地点
1

研究概览

简要总结

Topiramate (TPM) is an antiepileptic drug with a unique mode of action that is often useful in patients refractory to other drugs. However its use is restricted by the high incidence of cognitive adverse drug reactions (ADRs) that are associated with TPM exposure. TPM has been shown to cause particular cognitive ADRs, characterized by verbal fluency, attention, working memory and language deficits, at a much higher rate than other antiepileptic drugs. There do not appear to be obvious differences between patients that do or do not experience cognitive ADRs when on TPM (e.g. age, sex, concomitant medications, diagnosis), which suggests a genetic contributor.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
17 Years 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • adult (>17 years old) patients with epilepsy or patients with migraine treated by topiramate

排除标准

  • allergy to topiramate
  • abnormal liver or renal function

研究者

申办方类型
Other

研究点 (1)

Loading locations...

相似试验