EUCTR2007-004297-40-GB进行中（未招募）1 期
Pharmacological treatment of nystagmus: A randomised double masked placebo controlled crossover study using gabapentin and memantine. - Pharmacological treatment of nystagmus 3
niversity Hospitals of Leicester NHS Trust0 个研究点目标入组 180 人开始时间: 2007年10月15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）
- 发起方
- 入组人数
- 180
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
入选标准
- •Patients with cingenital or acquired nystagmus over the age of 16 years.
- •Are the trial subjects under 18? yes
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Patients with contraindication for gabapentin or memantine such as epilepsy, renal impairment, pregnancy or breast-feeding. For women of childbearing potential, a pregnancy test will be performed and documentation of adequate contraception during the study drug administration will be obtained. Patients on medication incompatible with gabapentin or memantine, such as amantadin.
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