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临床试验/JPRN-UMIN000030038
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Exploratory study for dry eye patient satisfaction with treatment - Exploratory study for dry eye patient satisfaction with treatment

Santen Pharmaceutical Co., Ltd.0 个研究点目标入组 100 人开始时间: 2017年11月20日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
100

研究概览

简要总结

Inclusion for Analysis: 100 cases [20 males,80 females, Age:70.7 plus or minus 11.2, Elapsed time since diagnosis of dry eye: 62.7 plus or minus 35.7 months] Treatment satisfaction: Very satisfied 10.0%, satisfied 43.0%, normal 44.0%, dissatisfied 3.0%. Factor analysis of satisfaction [the most important reason for satisfaction]: moisture feeling 29.0%, dryness improvement 19.0%, foreign body sensation improvement 15.0%. Relationship between patient background and ophthalmic findings / symptoms: No clear correlation was found. DEQS score: 13.6 plus or minus 13.3, BUT: 3.9 plus or minus 2.3 sec, corneal and conjunctival staining score: 2.2 plus or minus 1.9, LWE with 30.8%, conjunctival relaxation with 29.3%, SLK with 15.7%, Meibomian Gland abnormalities 80.8%.

研究设计

研究类型
Observational

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

  • Having advanced ocular disorder due to ocular pemphigus or Stevens Johnson syndrome Using a punctal plug and performing a punctal closure procedure Diquafosol sodium ophthalmic solution and sodium hyaluronate ophthalmic solution are used in combination. Treated with Rebamipide suspension eye drop Subject with hypersensitivity to fluorescein The investigator judges that the subject is ineligible as the study subject.

研究者

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