JPRN-jRCT1031210018招募中4 期
Effects of diquafosol sodium 3% versus hyaluronic acid 0.1% in patients with dry eye disease after cataract surgery: A single-center, randomized, controlled trial
Inomata Takenori0 个研究点目标入组 42 人开始时间: 2021年4月6日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 42
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
- >= 20age old 至 ot applicable(—)
- 性别
- Female
入选标准
- •1) Women over 20 years old
- •2) Patients who have undergone cataract surgery in both eyes within 14 days of completing the first eye
- •3) 3.Patients diagnosed with DED after cataract surgery (More than 13 points of J-OSDI total score and tear film breakup time less than 5 seconds)
- •4) 4.Patients who, after receiving a full explanation of their participation in the study and with a full understanding of the study, have given written consent of their own free will to participate in the study
- •5) In case of inability to self-administer eye drops, patients with a caregiver willing to and able to assist in administration of the assigned eye drop as part of the study
排除标准
- •1) Patients with dry eye diagnosed prior to cataract surgery (J-OSDI of 13 points or higher and tear layer breakup time of 5 seconds or less)
- •2) Patients with active eye infections
- •3) Spring catarrh patients
- •4) Patients with recurrent corneal erosions
- •5) Patients with hereditary corneal disease
- •6) Patients with physical irritation of the cornea and conjunctiva due to wear and tear or laxity of the ocular conjunctiva
- •7) Patients who cannot or will not be able to discontinue ophthalmic medications other than concomitantly restricted medications (including all prescription and OTC medications) from the initial screening examination to the end of the study medication eye drop
- •8) Patients who cannot stop using their contact lenses from the start of the screening examination until the end of the study drug eye drop
- •9) Patients after corneal refractive surgery
- •10) Patients with a teardrop plug or a history of surgical teardrop closure
- •11) Patients with hypersensitivity to the components of the study drug and the study's test product
- •12) Patients using glaucoma eye drops
- •13) Patients with systemic diseases, suchas diabetes mellitus, thyroid disease. Autoimmune diseases, and atopic dermatitis
- •14) Other patients who are deemed by the principal investigator to be unsuitable as research subjects
研究者
相似试验
已完成
不适用
Clinical Effects and Safety of 3% Diquafosol After Cataract SurgeryDry Eye SyndromesNCT02608489Soonchunhyang University Hospital86
已完成
不适用
Evaluation of efficacy of diquafosol sodium ophthalmic solution and sodium hyaluronate ophthalmic solution on treatment of dry eye (multicenter study).Dry eyeJPRN-UMIN000009071Ehime University200
尚未招募
不适用
Effects of 3% diquafosol sodium ophthalmic solution on visual function in patient with dry eye wearing contact lens.dry eyeJPRN-UMIN000010975Minamiaoyama Eye Clinic Tokyo20
已完成
不适用
Effect of the dual treatment of diquafosol sodium and rebamipide on dry eye syndrome related to chronic graft versus host disease and Sjogrens syndromeDry eye related to chronic GVHD and Sjogren s syndromeJPRN-UMIN000013234Keio University School of Medicine20
已完成
不适用
Effect of diquafosol sodium on treatment of dry eye associated with chronic graft-versus-host diseaseJPRN-UMIN000006862Department of Ophthalmology, Keio University School of Medicine50
