JPRN-UMIN000006621已完成未知
Clinical evaluation of tafluprost and travoprost in Japanese patients with primary open angle glaucoma or ocular hypertension: multicenter, randomized, 12-week crossover study - Clinical evaluation of tafluprost and travoprost in glaucoma patients
Hiroshima uiversity0 个研究点目标入组 220 人开始时间: 2011年10月30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
- 220
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. Patinets who with a history of allergy (i.e. hypersensitivity) to the drugs to be used during the study period. 2. Females who are pregnant, nursing or planning a pregnancy, or females of childbearing potential. 3. Patients who with a history of corneal refractive surgery. 4. Patinets who need wearing contact lenses during the study period. 5. Patinets who with extraocular disease, inflammation or infection in the eye(s) or eyelid(s). 6. Patinets who with a history of cataract surgery within 12 months. 7. Patinets who with a history of intraocular surgery including ocular laser treatment against glaucoma within 12 months 8. Patinets who has been treated with prostaglandin/timolol malate fixed combination. 9. Patinets who has been treated with prostaglandin generic drug. 10. Patinets who is treated dry eye therapy (drug medication, punctum plug and punctum occlusion). 11. Patinets who the investigator consider ineligible for enrolment
研究者
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