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临床试验/NCT04680143
NCT04680143已完成1 期

Systemic Erythropoietin Injection in Patients Having Optic Atrophy

Alexandria University1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2020年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
10
试验地点
1
主要终点
Visual acuity

研究概览

简要总结

The purpose of this treatment trial is to study the effect of systemic erythropoietin in patients having optic atrophy.

详细描述

The purpose of this treatment trial is to study the effect of systemic erythropoietin in patients having optic atrophy. The intervention is systemic erythropoietin injections (eprax 10000 IU subcutaneous twice daily for three days).

Follow up after one month and three months by recording visual acuity and electro physiological studies.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Post papilledemic optic atrophy patients

排除标准

  • Refuse to give an informed consent

研究组 & 干预措施

Systemic erythropoietin injections

Experimental

The study included 10 patients diagnosed as post papilledemic optic atrophy

干预措施: Systemic erythropoietin injection (Drug)

结局指标

主要结局

Visual acuity

时间窗: 3 months

VIsual acuity assessed at the follow up

Pattern visual evoked Potential .

时间窗: 3 months

Pattern visual evoked Potential .in both eyes to use data of the normal fellow eye as patients' internal control

Pattern electroretinogram

时间窗: 3 months

Pattern electroretinogram in both eyes to use data of the normal fellow eye as patients' internal control

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohamed Fahmy Doheim

Prinicipal investigator

Alexandria University

研究点 (1)

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