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临床试验/JPRN-UMIN000002717
JPRN-UMIN000002717已完成未知

Study of low-responder to Tafluprost ophthalmic solution and Latanoprost ophthalmic solution - Study of low-responder to Tafluprost ophthalmic solution and Latanoprost ophthalmic solution

Kyoto University Hospital Department of Ophthalmology and visual sciences0 个研究点目标入组 100 人开始时间: 2010年1月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
100

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) Having any hypersensitivity to test drugs. 2) Having severe visual field defect (HFA <-15dB) 3) Having absolute scotoma within 5 degrees in the center of the visual field. 4) Having any corneal abnormality or other condition preventing reliable applanation tonometry. 5) Having history of glaucoma surgery. 6) Having history of cataract surgery within 1 year. 7) Having history of refractive surgery. 8) Presence of any external ocular disease, inflammation or infection of the eye and/or eyelids. 9) Subjects need to be treated with corticosteroid during study period. 10) Pregnant subjects and subjects suspected of being pregnant 11) Subjects investigators declare ineligible for any sound medical reason

研究者

发起方
Kyoto University Hospital Department of Ophthalmology and visual sciences

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