跳至主要内容
临床试验/NCT00302991
NCT00302991已完成不适用

Quality of Life and Adverse Effects in Epilepsy Patients According to Treatment Group (EPIKA)

UCB Pharma0 个研究点目标入组 180 人开始时间: 2006年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
UCB Pharma
入组人数
180

研究概览

简要总结

Observational, multicentre, epidemiological study to determine the HRQOL of patients with epilepsy according to treatment sub-group and to validate the Spanish version of the Adverse Events Profile, produced by G. Baker et al. Three treatment groups will be examined: patients receiving only a new anti-epilepsy drug (AED), patients receiving a "classic" AED; patients receiving combination therapy.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

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

入选标准

  • Epileptic adult patients treated at a stable dose with one or more AEDs for ≥ 3 months

排除标准

  • Symptomatic epilepsy due to malignant brain tumour or progressive brain disease.
  • Confirmed diagnosis of a concomitant chronic disease

研究者

发起方
UCB Pharma
申办方类型
Industry

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