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临床试验/NCT00471068
NCT00471068终止4 期

Study of Travatan and Cosopt in Primary Open-Angle Glaucoma or Ocular Hypertension

Alcon Research1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2007年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
46
试验地点
1
主要终点
Intaocular Pressure (IOP) Mean Change After 6 Weeks of Treatment

研究概览

简要总结

To compare the efficacy and safety in patients treated with travoprost versus dorzolamide/timolol maleate combination in patients with open-angle glaucoma or ocular hypertension

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with open-angle glaucoma or ocular hypertension

排除标准

  • 未提供

研究组 & 干预措施

Travatan

Experimental

Travatan: 6 weeks treatment with Travatan (travoprost 40 mg/ml eye drops, solution) once daily at 08:00 and placebo (timolol vehicle) once daily at 20:00 in the affected eye(s)

干预措施: Travatan (Drug)

Travatan

Experimental

Travatan: 6 weeks treatment with Travatan (travoprost 40 mg/ml eye drops, solution) once daily at 08:00 and placebo (timolol vehicle) once daily at 20:00 in the affected eye(s)

干预措施: Placebo (Timolol Vehicle) (Drug)

Cosopt

Active Comparator

treatment period of 6 weeks with Cosopt (dorzolamide 20 mg/ml and timolol maleate 5 mg/ml eye drops, solution) twice daily at 08:00 and 20:00 in the affected eye(s)

干预措施: Cosopt (Drug)

结局指标

主要结局

Intaocular Pressure (IOP) Mean Change After 6 Weeks of Treatment

时间窗: At week 0 and week 6

IOP measured at week 6 minus IOP measured at baseline

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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