JPRN-UMIN000016986已完成未知
The randomized controlled trial on Mucosta ophthalmic suspension UD2% of effect in cataract surgery for dry eye patients - The randomized controlled trial on Mucosta ophthalmic suspension UD2% of effect in cataract surgery for dry eye patients
The Ethical Review Board of Medical Association Ophthalmological Koseikai0 个研究点目标入组 30 人开始时间: 2015年3月31日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 30
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 complicated with any anterior segment disease other than dry eyes(including blepharitis, lagophthalmos,blepharospasm,and iritis ) (excluding past histories) 2. Patients unable to discontinue using contact lenses between the time of tests at the time of screening and the end of topical instillation of the study drug. 3. Patients with a lacrimal plug implanted or patients in whom a lacrimal opening plug dropped off within 3 months before the time of tests at the start of topical instillation. 4. Patients who perform a plan (hope) of the insertion of the Toric IOLs. 5. Patients with a history of ocular surface surgery within 12 months before tests at the start of topical instillation. 6. Patients with a severe eye disorder due to Stevens-Johnson syndrome or ocular pemphigoid. 7. Patients with hypersensitivity to any ingredient of the present study drug or reagent used in the present study. 8. Patients judged by the principal investigator/sub-investigator to be unable to be included in the study due to a previous or concurrent systemic disease. 9. Other patients judged by the principalinvestigator/sub-investigator to be not appropriate for safe implementation of the present study.
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