CTRI/2019/01/016844已完成4 期
A Prospective, Multicenter, Post-marketing Surveillance to Assess Safety & Efficacy of Perampanel in Indian Patients as an Adjunctive Treatment inPartial Onset Seizures with or Without Secondary Generalized Seizures in Patients with Epilepsy Aged 12 years or older.
Eisai Pharmaceutical India Limited0 个研究点目标入组 200 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 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
- Pms
入排标准
入选标准
- •1. Male or female patients age greater than or equal to 12 years at the time of informed
- •2. Patients prescribed perampanel for the adjunctive treatment of partial onset seizures
- •based on independent clinical judgment of treating physicians.
- •3. Patients who provide informed consent to the treating physician.
排除标准
- •1. Participation in another study involving administration of an investigational drug or
- •device whilst participating in this observational study
- •2. Hypersensitivity [allergic] to perampanel
研究者
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