JPRN-UMIN000023979已完成1 期
Phase 1/2 clinical trial to evaluate the safety and efficacy of daily intravitreal injections of KUS121 for three days in patients with non-arteritic central retinal artery occlusion - Phase 1/2 clinical trial of intravitreal injections of KUS121 in patients with central retinal artery occlusion
Kyoto University Hospital Institute for Advancement of Clinical and Translational Science0 个研究点目标入组 9 人开始时间: 2016年9月15日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 9
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 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1) Patients who reported one or more of the following conditions: severe complications from cardiac, hepatic, or renal disease; poorly controlled diabetes mellitus 2) Eyes with the following conditions: Acute ocular or periocular infection Uncontrolled intra ocular pressure despite medication Retinal venous occlusion Abnormality in the macula Opacity in the lens or the vitreous such that the fundus is not visible 3) Contralateral eye: BCVA <= 0.1, or visual field loss >= 1/2 of isopter I4e 4) Bilateral onset of CRAO 5) Systemic use of immunosuppressant or steroid medications 6) Participation in other studies during the period 16 weeks prior 7) Possibility or history of hypersensitivity reaction to fluorescein. 8) Inability to understand consent requirements, or unwillingness or inability to participate in all of the follow-up examinations 9) Decision by the principal investigator or the physician in charge that patient was unsuitable for participation in the present study
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