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
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.
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