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临床试验/EUCTR2016-004957-33-Outside-EU/EEA
EUCTR2016-004957-33-Outside-EU/EEA进行中(未招募)1 期

Comparative Study of Zonisamide and Carbamazepine as an Initial Monotherapy: Efficacy and Safety Evaluation

Eisai Korea Inc.0 个研究点目标入组 200 人开始时间: 2017年2月13日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Epilepsy participants over 15 years old.
  • 2. Occurrence of seizure should be more than one time within recent 3 months and more than two times within recent 6 months.
  • 3. Participants who have not taken antiepileptic drugs (AEDs) in recent 3 months.
  • 4. For women of childbearing potential, the participant must have agreed to use contraception during the study period.
  • 5. Participants who agree with Informed Consent Form.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 200
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 200
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Participants who have Myoclonic seizures and/or Absence seizures.
  • 2. Participants who have progressive central nervous system (CNS) disorder.
  • 3. Participants who have serious systemic disorder.
  • 4. Participants with serum glutamic oxaloacetic transaminase (SGOT)/serum glutamic pyruvic transaminase (SGPT) level more than twice the normal range or blood urea nitrogen (BUN)/Creatinine level more than 3 times the normal range.
  • 5. Participants who have renal stones.
  • 6. Medical history of medicinal poisoning and/or alcoholism.
  • 7. Participants who have long-term medication history (more than 6 months) of zonisamide and/or carbamazepine.

研究者

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