EUCTR2013-003431-29-IT进行中（未招募）不适用
A multicenter medical safety follow-up study for patients with partial onset seizures who received more than 28 days of total exposure to BGG492 in studies CBGG492A2207 and/or CBGG492A2212.
ovartis Farma S.p.A.0 个研究点目标入组 77 人开始时间: 2014年4月28日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 77
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.Written informed consent must be obtained before any assessment is performed;
- •2.Patients must be cooperative, willing to participate in the study assessments, and able to report adverse events themselves or have a caregiver who can record and report the events;
- •3.Total exposure to BGG492 treatment in study CBGG492A2207 and/or CBGG492A2212 must have been greater than 28 days;
- •4.At least one year must have elapsed since the patient received his or her last dose of BGG492.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 60
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 17
排除标准
- •There are no exclusion criteria for this study so that all patients meeting the inclusion criteria will be eligible to participate in the medical follow-up assessments.
研究者
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