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临床试验/NCT00275925
NCT00275925已完成4 期

A 24-Week Prospective, Open-Label, Multicenter Study to Evaluate the Effect on Seizure Frequency, Safety and Tolerability of Oxcarbazepine Monotherapy in Adult Patients With Partial Seizures

Novartis14 个研究点 分布在 2 个国家目标入组 80 人开始时间: 2005年12月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
Novartis
入组人数
80
试验地点
14
主要终点
Epileptic activity at electroencephalography in rest

研究概览

简要总结

This study is aimed to evaluate the efficacy, safety and tolerability of oxcarbazepine monotherapy in adults with partial seizures.

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
Treatment
盲法
None

入排标准

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

入选标准

  • males and females, 18 - 70 years of age;
  • diagnosis of epilepsy, partial seizures;
  • ineffective or intolerable present therapy with 1 antiepileptic drug, or none of previous therapy with antiepileptic drugs

排除标准

  • progressive lesion of brain revealed by CT/MRI that performed no earlier than 2 years prior to screening;
  • non-epileptic seizures;
  • drug or alcohol dependence during a year prior to screening;
  • Other protocol-defined inclusion/exclusion criteria may apply.

结局指标

主要结局

Epileptic activity at electroencephalography in rest

Flash light and hyperventilation test with electroencephalography

Frequency of epileptic episodes according to patient's diary

Electrocardiogram analysis for rhythm and conduction

Blood test for sodium, hepatic enzymes and blood cells

次要结局

  • Quality of Life assessment at baseline, last visit
  • Tolerability and safety of 24 week's treatment with oxcarbazepine monotherapy in adult patients with partial seizures
  • Rate of patients with total and partial control of epilepsy
  • Rate of patients requiring additional antiepileptic drugs

研究者

发起方
Novartis
申办方类型
Industry

研究点 (14)

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