JPRN-UMIN000021887已完成2 期
Voluntary clinical trials to examine the safety and efficacy of transdermal electrical stimulation intended for retinitis pigmentosa - Transdermal electrical stimulation intended for retinitis pigmentosa
Chiba university Department of Ophthalmology0 个研究点目标入组 6 人开始时间: 2016年4月12日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 6
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 80years-old(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •Patients conflict with one of the following: 1)Patients with vitreous macular traction syndrome, macular edema, epiretinal membrane, macular lesions such as high myopia with posterior staphyloma 2)Patients undergoing eye surgery within three months 3)Patients who use isopropyl unoprostone, calcium antagonist, dark adaptation improving agent within 31 days 4)Patient with a history of drug allergy for mydriatic, such as eye drops anesthetic that we plan to use during the trial period 5)Patients who are complicated by diabetic retinopathy 6)patients with merging inflammation external eye, infections, or severe dry eye 7)Patients likely to have been pregnant or pregnant. Patients during breast-feeding. Patients who wish to become pregnant during the study period 8)Patients with a history of optic nerve disease 9)Patients with merger moderate (grade3 of Emery classification) or more of nuclear cataract, serious affect such pre subcapsular cataract, posterior subcapsular cataract or secondary cataract in vision
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