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临床试验/NCT01376180
NCT01376180已完成不适用

Drug Use Investigation for LAMICTAL

GlaxoSmithKline0 个研究点目标入组 3,000 人开始时间: 2008年12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
3,000
主要终点
The number of adverse events in Japanese subjects with epilepsy treated with lamotrigine tablet

研究概览

简要总结

The purpose of this study is to grasp actual status of usage of lamotrigine tablet and to collect information for using lamotrigine tablet effectively and safely as well as to grasp onset status of adverse events in pediatric subjects, geriatric subjects, pregnant women, subjects with poor renal and hepatic functions.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Subjects with epilepsy having the following seizure types.
  • Partial seizures (including secondary generalized seizures)
  • Tonic-clonic seizures
  • Generalized seizures of Lennox-Gastaut syndrome

排除标准

  • 未提供

研究组 & 干预措施

Subjects prescribed lamotrigine tablet

Subjects with epilepsy prescribed lamotrigine tablet during study period

干预措施: Lamotrigine (Drug)

结局指标

主要结局

The number of adverse events in Japanese subjects with epilepsy treated with lamotrigine tablet

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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